Human Insulin Injection
Human insulin injection is a replacement insulin used to improve blood sugar control in adults and children with diabetes mellitus.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 5 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Human insulin copies the body’s own insulin, lowering blood sugar in adults and children with diabetes by helping muscle and fat cells take in glucose and telling the liver to make less, and since about 1991 it has been the lower-cost alternative to newer insulins, with some forms sold without a prescription. Most people tolerate it well; besides low blood sugar, the usual complaints are weight gain and redness or itching where they inject. The one thing to watch for is low blood sugar, so learn the signs (shakiness, sweating, confusion) and keep juice or glucose tablets handy. Never share a pen or syringe, even with a new needle.
Clinical pearls
- Inject about 30 minutes before a meal, and never inject and then skip or delay that meal.
- Several strengths and mixes exist, including concentrated U-500, so check the label every time to avoid a dangerous mix-up.
- Rotate sites across the abdomen, thighs, buttocks and upper arms to prevent dimpled or thickened skin that absorbs insulin unevenly.
- Beta-blockers (heart and blood pressure drugs) and clonidine can hide low blood sugar warning signs, so test your sugar more often.
Patient information guide A plain-language walkthrough of Human Insulin Injection, written from its FDA label.
What Human Insulin Injection is used for
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Human insulin injection is used to improve blood sugar (glycemic) control in people with diabetes mellitus. Specific approvals depend on the product:
- Novolin 70/30 is approved for adults and pediatric patients with diabetes mellitus — it is a fixed mixture of intermediate-acting and short-acting human insulin and cannot be split into separate basal and mealtime doses
How Human Insulin Injection works
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Human insulin works by mimicking your body's own insulin. It signals muscles and fat tissue to absorb glucose from the blood, slows the liver's release of glucose, and helps your body use glucose for energy rather than breaking down fat or muscle. The combined effect is lower blood sugar. Insulin also supports protein building and prevents excess fat breakdown.
Human Insulin Injection dosage
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Novolin is injected subcutaneously (just under the skin) roughly 30 minutes before a meal. Your dose is individualized — your prescriber sets it based on your blood sugar readings, eating habits, activity level, and overall health. There is no one-size-fits-all schedule.
- Inject into the abdomen, thigh, buttock, or upper arm — rotate sites each time
- Novolin 70/30's fixed ratio means it cannot be adjusted separately for background or mealtime insulin needs
- If your regimen, dose, or injection sites change, monitor your blood sugar more often and follow your prescriber's guidance
Dosing details from the FDA-approved label
From the Human Insulin Injection prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Subcutaneous injection
- Inject subcutaneously approximately 30 minutes prior to the start of a meal into the abdominal area, buttocks, thigh, or the upper arm
- Rotate injection sites within the same region from one injection to the next
- Individualize and adjust the dosage based on route of administration, the individual's metabolic needs, blood glucose monitoring results and glyce
- Dosage adjustments may be needed with changes in physical activity, changes in meal patterns, changes in renal or hepatic function or during acute illness
- Intravenous administration
- Administer intravenously ONLY under medical supervision with close monitoring of blood glucose and potassium levels
- Dilute to concentrations from 0.05 unit/mL to 1 unit/mL insulin in infusion systems using polypropylene infusion bags
- Intravenous infusion bags are stable at room temperature for 24 hours
- Mixing with NOVOLIN N for subcutaneous injection
- NOVOLIN R can be mixed with NOVOLIN N
- NOVOLIN R should be drawn into the syringe first and the mixture should be injected immediately after mixing
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION • See Full Prescribing Information for important administration instructions. ( 2.1 ) • Subcutaneous injection: inject subcutaneously 30 minutes before a meal into the abdominal area, buttocks, thigh or the upper arm. Rotate injection sites to reduce risk of lipodystrophy and localized cutaneous amyloidosis. ( 2.2 ) • Intravenous use: administer intravenously ONLY under medical supervision at concentrations from 0.05 unit/mL to 1 unit/mL in infusion systems using polypropylene infusion bags. ( 2.2 ) • Individualize dose based on route of administration, metabolic needs, blood glucose monitoring results and glycemic control goal. ( 2.3 ) • NOVOLIN R given by subcutaneous injection should generally be used in regimens with an intermediate- or long-acting insulin. ( 2.3 ) • Can be mixed with NOVOLIN N. ( 2.5 ) 2.1 Important Administration Instructions Always check insulin labels before administration [see Warnings and Precautions ( 5.4 )]. • Inspect NOVOLIN R visually before use. It should appear clear and colorless. Do not use NOVOLIN R if particulate matter or coloration is seen. • Use of NOVOLIN R in insulin pumps is not recommended because of the risk of precipitation. 2.2 Route of Administration Subcutaneous Administration • Inject NOVOLIN R subcutaneously approximately 30 minutes prior to the start of a meal into the abdominal area, buttocks, thigh, or the upper arm. • Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy and localized cutaneous amyloidosis. Do not inject into areas of lipodystrophy or localized cutaneous amyloidosis [see Warnings and Precautions ( 5.2 ), Adverse Reactions ( 6 )]. Intravenous Administration • Administer NOVOLIN R intravenously ONLY under medical supervision with close monitoring of blood glucose and potassium levels to reduce the risk of hypoglycemia and hypokalemia [see Warnings and Precautions ( 5.3 , 5.6 ) and How Supplied/Storage and Handling ( 16.2 )] . • Dilute NOVOLIN R to concentrations from 0.05 unit/mL to 1 unit/mL insulin in infusion systems using polypropylene infusion bags. NOVOLIN R is stable in infusion fluids such as 0.9% sodium chloride, 5% dextrose, or 10% dextrose with 40 mmol/L potassium chloride. Intravenous infusion bags are stable at room temperature for 24 hours.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Human Insulin Injection side effects
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The most common side effect of human insulin is low blood sugar (hypoglycemia). Other reactions to be aware of include:
Common side effects
- Low blood sugar (hypoglycemia) — the most common reaction
- Redness, swelling, or itching at the injection site
- Skin changes at injection sites (lipodystrophy — dimpling or thickening)
- Weight gain
- Swelling (edema), especially in the hands or feet
- Low potassium levels (hypokalemia)
- Temporary changes in vision when starting or intensifying insulin therapy
- Redness, swelling, or itching at the injection site — usually clears up within days to weeks
- Weight gain from insulin's anabolic (tissue-building) effects
- Temporary blurry vision or eye changes when starting or intensifying treatment
When to get medical help
- Severe low blood sugar — get help immediately if you have seizures, loss of consciousness, or cannot treat it yourself
- Severe allergic reaction — seek emergency care for body-wide rash, difficulty breathing, fast heartbeat, low blood pressure, or sweating
- Dangerously low potassium (hypokalemia) — can cause irregular heartbeat or breathing problems
- Signs of heart failure — sudden weight gain, swelling, or shortness of breath (especially if also taking a thiazolidinedione diabetes pill)
- Call your doctor if your blood sugar is consistently too high or too low, or if you notice skin changes at injection sites
Severe low blood sugar, a serious drop in potassium, or a whole-body allergic reaction (anaphylaxis) require immediate medical attention.
Human Insulin Injection warnings and precautions
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- Hypoglycemia (low blood sugar) is the most serious and most common risk — it can cause seizures, unconsciousness, or death if untreated; know the signs and always carry a fast-acting carbohydrate
- Patients with kidney disease, liver disease, or older adults are at higher risk of low blood sugar and need more frequent monitoring
- Low potassium (hypokalemia) is a rare but life-threatening complication; tell your doctor if you take potassium-lowering medicines
- A severe allergic reaction (anaphylaxis) is possible — stop the medication and get emergency help if you develop widespread rash, trouble breathing, rapid heartbeat, or a sudden drop in blood pressure
- Thiazolidinedione diabetes pills used alongside insulin can cause fluid buildup and may worsen or trigger heart failure — report sudden swelling or shortness of breath to your doctor right away
- Never share a Novolin pen, needle, or syringe with another person — sharing can spread serious blood-borne infections
- Always check the insulin label before injecting — mix-ups between insulin products have caused dangerous errors
Human Insulin Injection interactions
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Several medications can meaningfully change how human insulin affects your blood sugar:
- Increases low-blood-sugar risk: other diabetes drugs, ACE inhibitors, blood pressure medications (angiotensin receptor blockers), certain antidepressants (MAO inhibitors, fluoxetine), fibrates, salicylates (like aspirin in high doses), and octreotide
- Reduces insulin's blood-sugar-lowering effect: corticosteroids, diuretics, estrogens, oral contraceptives, certain antipsychotics (olanzapine, clozapine), niacin, thyroid hormones, and growth hormone (somatropin)
- Unpredictable effect (up or down): alcohol, beta-blockers, clonidine, and lithium
- May mask low-blood-sugar warning signs: beta-blockers, clonidine, guanethidine, and reserpine — making it harder to notice when your blood sugar drops
- TZD diabetes pills (thiazolidinediones) used with insulin can cause fluid retention and heart failure
Interactions listed in the FDA-approved label
From the Human Insulin Injection prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Antidiabetic agents, ACE inhibitors, angiotensin II receptor blocking agents, disopyramide, fibrates, fluoxetine, monoamine oxidase inhibitors, pentoxifylline, pramlintide, salicylates, somatostatin analog (e.g., octreotide), sulfonamide antibiotics: May increase the risk of hypoglycemia. Dose adjustment and increased frequency of glucose monitoring may be required.
- Atypical antipsychotics (e.g., olanzapine and clozapine), corticosteroids, danazol, diuretics, estrogens, glucagon, isoniazid, niacin, oral contraceptives, phenothiazines, progestogens, protease inhibitors, somatropin, sympathomimetic agents (e.g., albuterol, epinephrine, terbutaline), thyroid hormones: May decrease the blood glucose lowering effect of the insulin. Dose adjustment and increased frequency of glucose monitoring may be required.
- Alcohol, beta-blockers, clonidine, and lithium salts: May increase or decrease the blood glucose lowering effect of the insulin. Dose adjustment and increased frequency of glucose monitoring may be required.
- Pentamidine: May cause hypoglycemia, which may sometimes be followed by hyperglycemia. Dose adjustment and increased frequency of glucose monitoring may be required.
- Beta-blockers, clonidine, guanethidine, and reserpine (antiadrenergic drugs): May blunt signs and symptoms of hypoglycemia; signs and symptoms may be reduced or absent. Increased frequency of glucose monitoring may be required.
Read the label’s full interactions text
7 DRUG INTERACTIONS Table 1: Clinically Significant Drug Interactions with NOVOLIN 70/30 Drugs that May Increase the Risk of Hypoglycemia Drugs: Antidiabetic agents, ACE inhibitors, angiotensin II receptor blocking agents, disopyramide, fibrates, fluoxetine, monoamine oxidase inhibitors, pentoxifylline, pramlintide, salicylates, somatostatin analog (e.g., octreotide), and sulfonamide antibiotics Intervention: Dose adjustment and increased frequency of glucose monitoring may be required when NOVOLIN 70/30 is co-administered with these drugs. Drugs that May Decrease the Blood Glucose Lowering Effect of NOVOLIN 70/30 Drugs: Atypical antipsychotics (e.g., olanzapine and clozapine), corticosteroids, danazol, diuretics, estrogens, glucagon, isoniazid, niacin, oral contraceptives, phenothiazines, progestogens (e.g., in oral contraceptives), protease inhibitors, somatropin, sympathomimetic agents (e.g., albuterol, epinephrine, terbutaline), and thyroid hormones. Intervention: Dose adjustment and increased frequency of glucose monitoring may be required when NOVOLIN 70/30 is co-administered with these drugs. Drugs that May Increase or Decrease the Blood Glucose Lowering Effect of NOVOLIN 70/30 Drugs: Alcohol, beta-blockers, clonidine, and lithium salts. Pentamidine may cause hypoglycemia, which may sometimes be followed by hyperglycemia. Intervention: Dose adjustment and increased frequency of glucose monitoring may be required when NOVOLIN 70/30 is co-administered with these drugs. Drugs that May Blunt Signs and Symptoms of Hypoglycemia Drugs: Beta-blockers, clonidine, guanethidine, and reserpine Intervention: Increased frequency of glucose monitoring may be required when NOVOLIN 70/30 is co-administered with these drugs. • Drugs that Affect Glucose Metabolism: Adjustment of insulin dosage may be needed. ( 7 ) • Antiadrenergic Drugs (e.g., beta-blockers, clonidine, guanethidine, and reserpine): Signs and symptoms of hypoglycemia may be reduced or absent. ( 5.3 , 7 )
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Human Insulin Injection
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- Do not use Novolin if your blood sugar is already low (hypoglycemia) — insulin will make it worse
- Do not use Novolin if you have had a serious allergic reaction to it or any of its ingredients
- Tell your prescriber about kidney or liver problems — both raise your risk of low blood sugar and may require dose changes
- Older adults are at increased risk of hypoglycemia due to other health conditions — closer monitoring is recommended
- Children can use Novolin, but doses must be tailored carefully with frequent blood sugar checks
- Pregnancy: available studies do not show human insulin causes birth defects, but poorly controlled diabetes in pregnancy poses real risks to mother and baby — work closely with your doctor
- Breastfeeding: human insulin may pass into breast milk; discuss with your doctor whether to continue or adjust therapy
Human Insulin Injection overdose
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Too much insulin causes low blood sugar (hypoglycemia) — and if given intravenously, it can also dangerously lower potassium. Mild cases can be treated by eating or drinking fast-acting sugars. Severe cases involving seizures or unconsciousness may need glucagon injections or intravenous glucose under medical care. Low blood sugar can return even after you feel better, so monitoring and additional carbohydrates are often needed.
What Human Insulin Injection does in the body
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Human insulin's main job is lowering blood glucose. After a subcutaneous injection of Novolin R, the glucose-lowering effect begins around 30 minutes, peaks between 1.5 and 3.5 hours, and lasts about 8 hours. The exact timing can vary between people and even in the same person on different days — factors like injection site, blood flow, and body temperature all play a role. Novolin R has a slower onset and longer action than rapid-acting insulin analogs.
How your body processes Human Insulin Injection
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After a subcutaneous dose of Novolin R, insulin levels in the blood peak roughly 1.5 to 2.5 hours after injection and return to baseline around 5 hours post-dose. The effects of age, sex, obesity, kidney disease, and liver disease on how the body handles Novolin R have not been formally studied, so closer monitoring is advised in those groups.
How to store Human Insulin Injection
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Dispense in the original sealed carton with the enclosed Instructions for Use. Do not freeze. store without a needle attached.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Human Insulin Injection
259 supplements and herbal products have documented interactions with Human Insulin Injection in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 3
- Moderate · 218
- Minor · 38
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Nutrient depletion considerations
Human Insulin Injection has been associated with lower levels of 2 nutrients in the clinical literature. This does not mean a deficiency will occur — it means these may be worth discussing with your pharmacist or healthcare provider, especially with long-term use.
Educational information from a licensed clinical database (Natural Medicines) — not medical advice. Do not start or stop medications or supplements without professional guidance.
Human Insulin Injection: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Human Insulin Injection — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly is Novolin and why was I prescribed it?
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How do I take this injection, and does it matter when I eat?
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What does low blood sugar feel like, and what should I do if it happens?
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Are there any medications or foods I need to avoid while taking this insulin?
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Is it safe to use insulin if I'm pregnant or breastfeeding?
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Can I share my Novolin pen or needles with a family member who also uses insulin?
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Is Human Insulin Injection available over the counter?
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When was Human Insulin Injection first available?
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Who makes Human Insulin Injection?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Human Insulin Injection on HelloPharmacist
Human Insulin Injection forms and strengths (how it comes)
Human Insulin Injection is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Injection
How this form is used
- Novolin 70/30 is used to improve blood sugar control in adults and children with diabetes mellitus
- Novolin 70/30 contains a fixed mix of intermediate-acting and short-acting human insulin — the ratio cannot be separated for basal or mealtime adjustments
- Novolin subcutaneous injection is given about 30 minutes before a meal into the abdomen, thigh, buttock, or upper arm
- Rotate injection sites within the same body region each time to reduce the risk of skin changes
- Do not inject into areas of skin thickening or dimpling (lipodystrophy)
- Always inspect Novolin before use — it should look clear and colorless; do not use it if you see particles or discoloration
Human Insulin Injection on the U.S. market: products, makers and brands
How Human Insulin Injection appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
2 companies list 7 Human Insulin Injection product records with the FDA, mostly as injection; the earliest marketing or approval year on record is 1991. Brand names on the directory include Humulin 70/30, Humulin N, Humulin R U-500 and 8 more; the rest are generics.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
How widely Human Insulin Injection is used (Medicaid data)
A general measure of how commonly Human Insulin Injection is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Human Insulin Injection is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Human Insulin Injection prescribed? Of the 1,601 medications we measure, Human Insulin Injection ranks #284 by Medicaid prescriptions — more than 82% of them.
Utilization by Human Insulin Injection product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
insulin, regular, human 100 UNT/ML Injectable Solution Most dispensed
Summed across the 9 of 35 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 311034
3 ML insulin, regular, human 500 UNT/ML Pen Injector
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1731315
3 ML insulin, regular, human 100 UNT/ML Pen Injector
Summed across the 2 of 4 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2206090
insulin, regular, human 500 UNT/ML Injectable Solution
Summed across the 1 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 249220
100 ML insulin, regular, human 1 UNT/ML Injection
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2179744
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Human Insulin Injection, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 14 of 47 listed Human Insulin Injection NDCs with Medicaid activity.
Compare Human Insulin Injection products
A representative set of FDA-listed product records for Human Insulin Injection — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Injection | ||||
| 100 [IU]/mL | Subcutaneous | A-S Medication Solutions | BLA | View NDC → |
| 100 [IU]/mL | Subcutaneous | Novo Nordisk × 6 listings | BLA | View NDC → |
Showing 7 of 7 products — FDA National Drug Code Directory. See every product, package size and price: browse all 7 Human Insulin Injection NDCs →
Human Insulin Injection side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Human Insulin Injection — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Human Insulin Injection in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Human Insulin Injection FDA approval history
How Human Insulin Injection went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Human Insulin Injection recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Human Insulin recalls since July 2021.
✅No Human Insulin recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 253182 4 dose forms · 8 strengths
-
Dose form (SCDF) Inhalation Powder RxCUI 2108525No current FDA listing -
Dose form (SCDF) Injectable Solution RxCUI 376915In current FDA listings -
Dose form (SCDF) Injection RxCUI 2179743In current FDA listingsClinical drug / strength (SCD) 100 ML insulin, regular, human 1 UNT/MLRxCUI 2179744 -
Dose form (SCDF) Pen Injector RxCUI 1731314In current FDA listingsClinical drug / strength (SCD) 3 ML insulin, regular, human 100 UNT/MLRxCUI 22060903 ML insulin, regular, human 500 UNT/MLRxCUI 1731315
Look up RxCUI 253182 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Human Insulin Injection supply and shortage status
Whether Human Insulin Injection is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Human Insulin Injection costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Injection, Suspension · Subcutaneous | 100 [IU]/mL | $4.62 per mL | NDC details & price history |
| Injection, Solution · Subcutaneous | 100 [IU]/mL | $4.62 per mL | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Human Insulin Injection brand names
Human Insulin Injection is sold under 11 brand names in the FDA directory — Humulin 70/30, Humulin N, Humulin R U-500, Humulin R and others. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Human Insulin Injection: manufacturers and labelers
2 companies list Human Insulin Injection products with the FDA. By number of product records, the largest are Novo Nordisk, A-S Medication Solutions. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Human Insulin Injection drug class (RxNorm)
Human Insulin Injection belongs to the Insulin class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Human Insulin Injection page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Novo Nordisk is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →