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anti diarrheal anti gas loperamide hydrochloride, simethicone 2 mg; 125 mg Tablet, 30-count — NDC 37808-0714-65 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

anti diarrheal anti gas loperamide hydrochloride, simethicone 2 mg; 125 mg Tablet, 30-count — NDC 37808-714-65 (Billing 37808-0714-65)

by H E B · 1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE

This is a package of 30 tablets of anti diarrheal anti gas loperamide hydrochloride, simethicone 2 mg; 125 mg Tablet from H E B, no longer marketed (first marketed Nov 2018), no longer in the FDA NDC Directory.

NDC 37808-0714-65
🏷️ FDA NDC (as labeled) 37808-714-65 billing pads the product segment with a zero
This package
Contains30-count Pack sizes3 compare ↓
Product page 37808-0714-53 Also comes in: 12 tablets 37808-714-53 24 tablets 37808-714-62
OTC Generic Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 37808-714-65
Product NDC 37808-714
11-digit billing NDC 37808071465
RxCUI 978001
UNII 77TI35393C, 92RU3N3Y1O
Application # ANDA209837
SPL Set ID 35cff261-932e-4b2e-ab21-80969c27fa92
Physiologic effect Skin Barrier Activity
DEA schedule Non-controlled
Marketing category ANDA
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2018-11-15
Route ORAL
Dosage form TABLET
Substance LOPERAMIDE HYDROCHLORIDE; DIMETHICONE
Quick answers
  • RxCUI (RxNorm): 978001
Why two NDCs? The FDA registers this code as 37808-714-65 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 37808-0714-65. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Opioid Agonist class.

Pharmacologic class Opioid Agonist
Drug family (ATC) Antipropulsives
How it works Opioid Agonists
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📖 What it is MedlinePlus · NLM

Nonprescription (over-the-counter) loperamide is used to control acute diarrhea (loose stools that come on suddenly and usually lasts less than 2 weeks), including travelers' diarrhea. Prescription loperamide is also used to control acute diarrhea and also ongoing diarrhea associated with inflammatory bowel disease (IBD; condition in which the lining of all or part of the intestine is swollen, irritated, or has sores). Prescription loperamide is also used to reduce the amount of fluid in people with ileostomies (surgery to create an opening for waste to leave the body through the abdomen). Lop...

Read the full MedlinePlus article ↗

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 12 tablets 24 tablets
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
37808-0714-53 37808-714-53 Main listing 12 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK 2018-11-15 — Active
37808-0714-62 37808-714-62 24 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK 2020-02-03 — Active
37808-0714-65 You're viewing this 1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE 2018-11-19 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This is a 30-count package — 1 bottle in 1 carton / 30 tablet in 1 bottle.
How does this package differ from NDC 37808-0714-53?
Both are anti diarrheal anti gas loperamide hydrochloride, simethicone 2 mg; 125 mg Tablet — the drug itself is identical. This page's package is the 30-count one, while NDC 37808-0714-53 is the 12 tablets package.
What NDC number is used to bill for this package of anti diarrheal anti gas loperamide hydrochloride, simethicone 2 mg; 125 mg Tablet?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
good sense anti diarrheal anti gas 2 mg/1; 125 mg 00113-0087-53 L. 12 tablets $0.286 — Availability likely —
good neighbor pharmacy anti diarrheal anti gas 2 mg/1; 125 mg 46122-0620-62 Amerisource 24 tablets $0.286 — Availability likely —
foster and thrive anti diarrheal anti gas 2 mg/1; 125 mg 70677-1105-01 Strategic 12 tablets $0.286 — Availability likely —
Good Sense Anti Diarrheal Anti Gas 2 mg/1; 125 mg 00113-1087-89 L. 18 tablets — — FDA listed —
anti diarrheal and anti gas 2 mg/1; 125 mg 00363-1830-53 Walgreen 12 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 00363-9606-75 WALGREEN 12 tablets — — FDA listed —
up and up anti diarrheal anti gas 2 mg/1; 125 mg 11673-0646-62 Target 24 tablets — — FDA listed —
signature care anti diarrheal anti gas 2 mg/1; 125 mg 21130-0183-62 Safeway 24 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 21130-0222-24 Better 24 tablets — — FDA listed —
Anti Diarrheal Anti Gas 2 mg/1; 125 mg 30142-0581-53 Kroger 12 tablets — — FDA listed —
anti diarrheal anti gas 2 mg/1; 125 mgthis 37808-0714-65 H 30 tablets — — Discontinued —
equaline anti diarrheal plus anti gas 2 mg/1; 125 mg 41163-0553-89 United 18 tablets — — FDA listed —
anti diarrheal plus anti gas 2 mg/1; 125 mg 41250-0375-55 Meijer 42 tablets — — Discontinued —
CareOne Diarrhea and Gas Control 2 mg/1; 125 mg 41520-0772-53 American 12 tablets — — FDA listed —
anti diarrheal anti gas 2 mg/1; 125 mg 42507-0699-53 HyVee 12 tablets — — FDA listed —
IMODIUM Multi-Symptom Relief 2 mg/1; 125 mg 50580-0338-12 Kenvue 12 tablets — — FDA listed —
Loperamide HCl and Simethicone 2 mg/1; 125 mg 51660-0069-06 Ohm 6 tablets — — FDA listed —
Loperamide Hydrochloride, Simethicone 2 mg/1; 125 mg 53041-0263-50 Guardian 6 tablets — — FDA listed —
Anti-Diarrheal/Anti-Gas 2 mg/1; 125 mg 53943-0263-33 Discount 24 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 55319-0052-75 Family 12 tablets — — FDA listed —
dg health anti diarrheal anti gas 2 mg/1; 125 mg 55910-0383-53 Dolgencorp, 12 tablets — — FDA listed —
antidiarrheal multi symptom relief 125 mg/1; 2 mg 56062-0511-62 Publix 24 tablets — — Discontinued —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 58602-0815-74 Aurohealth 6 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 58602-0868-76 Aurohealth 24 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 58602-0869-76 Aurohealth 24 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 62207-0739-69 Granules 12 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 69230-0325-04 Camber 4 tablets — — FDA listed —
Anti-Diarrheal/Anti-Gas 2 mg/1; 125 mg 69256-0265-31 Harris 12 tablets — — FDA listed —
Loperamide hydrochloride and Simethicone 2 mg/1; 125 mg 69452-0210-04 Bionpharma 6 tablets — — FDA listed —
Loperamide hydrochloride and Simethicone 2 mg/1; 125 mg 69452-0531-12 Bionpharma 24 tablets — — FDA listed —
anti diarrheal and anti gas 2 mg/1; 125 mg 69842-0644-53 CVS 12 tablets — — FDA listed —
Basic Care Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 72288-0001-62 Amazon.com 24 tablets — — FDA listed —
Anti-Diarrheal/Anti-Gas Caplets 2 mg/1; 125 mg 73581-0178-24 YYBA 24 tablets — — FDA listed —
Anti-Diarrheal/Anti-Gas Multi-Symptom Relief 2 mg/1; 125 mg 79903-0116-33 Wal-Mart 24 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 79903-0223-12 WALMART 12 tablets — — FDA listed —
Equate Anti Diarrheal Anti Gas Multi-Symptom Relief 2 mg/1; 125 mg 79903-0302-12 WALMART 12 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 80136-0384-24 NORTHEAST 24 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 2 mg/1; 125 mg 81522-0325-24 FSA 24 tablets — — FDA listed —
Loperamide Hydrochloride and Simethicone 125 mg/1; 2 mg 84441-0713-10 IMO-GEN 100 tablets — — FDA listed —
anti diarrheal anti gas 2 mg/1; 125 mg 11822-1003-01 Rite 42 tablets — — Discontinued —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2018
On the market since
Nov 2018
📍
2026
Currently FDA-listed
8 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color White
ShapeOval
ImprintL0R1;2;125
Size17 mm
ScoringScored — splits in 2
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerH E B
Application holderPERRIGO R AND D CO
FDA applicationANDA209837 (ANDA)
Labeler code37808
First marketedNov 2018
Product typeHuman Otc Drug
Portfolio264 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Uses relieves symptoms of diarrhea plus bloating, pressure and cramps, commonly referred to as gas

⏱️ Dosage and Administration 163 words ▾

Directions • drink plenty of clear fluids to help prevent dehydration caused by diarrhea • take only on an empty stomach (1 hour before or 2 hours after a meal) • take with a full (8 oz.) glass of water • find right dose on chart below. If possible, use weight to dose; otherwise, use age. adults and children 12 years and over 2 caplets after the first loose stool; 1 caplet after each subsequent loose stool; but no more than 4 caplets in 24 hours children 9-11 years (60-95 lbs) 1 caplet after the first loose stool; ½ caplet after each subsequent loose stool; but no more than 3 caplets in 24 hours children 6-8 years (48-59 lbs) 1 caplet after the first loose stool; ½ caplet after each subsequent loose stool; but no more than 2 caplets in 24 hours children 2-5 years (34 to 47 lbs) ask a doctor children under 2 years (up to 33 lbs) do not use

⚠️ Warnings 189 words ▾

Warnings Allergy alert: Do not use if you have ever had a rash or other allergic reaction to loperamide HCl Heart alert: Taking more than directed can cause serious heart problems or death Do not use • if you have bloody or black stool • if you have difficulty swallowing Ask a doctor before use if you have • fever • mucus in the stool • a history of liver disease • a history of abnormal heart rhythm Ask a doctor or pharmacist before use if you are taking a prescription drug. Loperamide may interact with certain prescription drugs.

When using this product tiredness, drowsiness or dizziness may occur. Be careful when driving or operating machinery. Stop use and ask a doctor if • symptoms get worse • diarrhea lasts for more than 2 days • you get abdominal swelling or bulging.

These may be signs of a serious condition. • you have difficulty swallowing the caplet If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

(1-800-222-1222)

📦 Storage and Handling 40 words ▾

Other information • each caplet contains: calcium 165 mg, sodium 3 mg • store between 20 ° -25 ° C (68 ° -77 ° F). Protect from light. • do not use if printed blister unit is broken or torn

🧪 Active Ingredient 12 words ▾

Active ingredients (in each caplet) Loperamide HCl 2 mg Simethicone 125 mg

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients acesulfame potassium, croscarmellose sodium, dibasic calcium phosphate, maltodextrin, microcrystalline cellulose, natural and artificial flavor, propylene glycol, stearic acid

🎯 Purpose 3 words ▾

Purposes Anti-diarrheal Anti-gas

📄 Do Not Use 17 words ▾

Do not use • if you have bloody or black stool • if you have difficulty swallowing

📄 Ask a Doctor Before Use If 28 words ▾

Ask a doctor before use if you have • fever • mucus in the stool • a history of liver disease • a history of abnormal heart rhythm

📄 Ask a Doctor or Pharmacist Before Use If 21 words ▾

Ask a doctor or pharmacist before use if you are taking a prescription drug. Loperamide may interact with certain prescription drugs.

📄 When Using This Product 17 words ▾

When using this product tiredness, drowsiness or dizziness may occur. Be careful when driving or operating machinery.

📄 Stop Use and Ask a Doctor If 41 words ▾

Stop use and ask a doctor if • symptoms get worse • diarrhea lasts for more than 2 days • you get abdominal swelling or bulging. These may be signs of a serious condition. • you have difficulty swallowing the caplet

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-719-9260

📄 Package Label / Principal Display Panel 47 words ▾

Package/Label Principal Display Panel Compare to Imodium ® Multi-Symptom Relief active ingredients Loperamide Hydrochloride and Simethicone Tablets, 2 mg/125 mg Anti-Diarrheal/Anti-Gas Multi-Symptom Relief Caplet Relieves symptoms of diarrhea plus Cramps & Pressure - Bloating - Gas actual size 24 CAPLETS* *Capsule-Shaped Tablets anti diarrheal anti gas image

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Anti Diarrheal Anti Gas (this brand).

Top reported reactions

Cerebrovascular Accident1

Reporter sex

1 reports
Male · 100%

Serious outcomes

Hospitalization1
Life-threatening1
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 12 tablets (37808-0714-53), 24 tablets (37808-0714-62). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
H E B is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 37808-0713-79 · H 37808-0716-16 · HEB →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.