HomeNDC LookupIngredientsLosartan Potassium › 60312-0960-00
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losartan potassium 100 mg Tablet, Film Coated, 97,000-count

by ORGANON PHARMA (UK) LIMITED · 1 BAG in 1 DRUM (60312-0960-0) / 97000 TABLET, FILM COATED in 1 BAG
NDC 60312-0960-00
🏷️ FDA NDC (as labeled) 60312-0960-0 billing pads the package segment with a zero
On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 60312-0960-0
Product NDC 60312-0960
11-digit billing NDC 60312096000
SPL Set ID dfa6e67e-d198-42c2-92bb-3018768b4e17
DEA schedule Non-controlled
Marketing category DRUG FOR FURTHER PROCESSING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1995-04-14
Dosage form TABLET, FILM COATED
Substance LOSARTAN POTASSIUM
Why two NDCs? The FDA registers this code as 60312-0960-0 — a 5-4-1 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 package segment → 60312-0960-00. 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.

🏭 Manufacturer & labeler

LabelerORGANON PHARMA (UK) LIMITED
Labeler code60312
First marketedApr 1995
Product typeDrug For Further Processing
Portfolio21 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.

🩺 Clinical

📗 Our plain-language guide HelloPharmacist
  • Losartan is mainly used to lower high blood pressure, which protects you from strokes and heart attacks over time. Depending on your situation, your doctor may also have prescribed...
  • What exactly is losartan supposed to do for me?
  • You can take losartan at any time of day that works for you, as long as you're consistent. Taking it with or without food is both fine — eating may slow things down a tiny bit, but...
  • Does it matter what time of day I take it, and can I take it with food?
📖 Read our full Losartan guide →
1
Nutrient depletion considerations

Losartan Potassium may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.

🧪 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.

💲 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.
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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Losartan Potassium 100 mg 65862-0203-30 Aurobindo 30 tablets $0.044 Availability likely
Losartan Potassium 100 mg 11788-0102-10 AiPing 1000 tablets $0.044 AB Availability likely
Losartan Potassium 100 mg 62332-0029-30 Alembic 30 tablets $0.044 AB Availability likely
Losartan Potassium 100 mg 82009-0044-10 Quallent 1000 tablets $0.044 AB Availability likely
Losartan potassium 100 mg 33342-0046-07 Macleods 30 tablets $0.044 AB Availability likely
Losortan Potassium 100 mg 50268-0506-15 AvPAK 1 tablet $0.044 AB Availability likely
Losartan Potassium 100 mg 68084-0348-01 American 1 tablet $0.044 AB Availability likely
Losartan potassium 100 mg 72205-0143-30 Novadoz 30 tablets $0.044 AB Availability likely
Losartan Potassium 100 mg 43547-0362-03 Solco 30 tablets $0.044 AB Availability likely
Losartan Potassium 100 mg 00904-7049-61 Major 1 tablet $0.044 AB Availability likely
Losartan Potassium 100 mg 72603-0342-01 NorthStar 90 tablets $0.044 AB Availability likely
LOSARTAN POTASSIUM 100 mg 64380-0935-04 Strides 30 tablets $0.044 AB Availability likely
Losartan Potassium 100 mg 42571-0112-10 Micro 1000 tablets $0.056 AB Discontinued
Cozaar 100 mg 78206-0123-01 Organon 30 tablets $6.144 AB Availability likely
Losortan Potassium 100 mg 63187-0072-30 Proficient 30 tablets AB FDA listed
Losartan Potassium 100 mg 63187-0708-30 Proficient 30 tablets AB FDA listed
Losartan Potassium 100 mg 71610-0083-30 Aphena 30 tablets AB FDA listed
Losartan Potassium 100 mg 71610-0465-30 Aphena 30 tablets AB FDA listed
Losartan Potassium 100 mg 50090-3403-00 A-S 90 tablets AB FDA listed
Losartan Potassium 100 mg 72865-0143-10 XLCare 1000 tablets AB FDA listed
LOSARTAN POTASSIUM 100 mg 72789-0165-90 PD-Rx 90 tablets AB FDA listed
Losartan potassium Tablets, 100 mg 63629-2428-01 Bryant 1000 tablets AB FDA listed
Losartan Potassium 100 mg 71335-1235-01 Bryant 30 tablets AB Discontinued
Losartan Potassium 100 mg 43063-0954-30 PD-Rx 30 tablets AB FDA listed
Losartan Potassium 100 mg 55154-2333-00 Cardinal 1 tablet AB FDA listed
losartan potassium 100 mgthis 60312-0960-00 ORGANON 97000 tablets FDA listed
Losartan Potassium 100 mg 29300-0146-01 Unichem 100 tablets AB FDA listed
Losartan Potassium 100 mg 50090-4712-00 A-S 90 tablets AB FDA listed
Losartan Potassium 100 mg 51655-0828-26 Northwind 90 tablets AB FDA listed
Losartan Potassium 100 mg 68071-3846-03 NuCare 30 tablets AB FDA listed
Losartan Potassium 100 mg 68180-0378-01 Lupin 100 tablets AB FDA listed
Losartan Potassium 100 mg 00615-7960-05 NCS 15 tablets AB FDA listed
Losartan Potassium 100 mg 63187-0808-30 Proficient 30 tablets AB FDA listed
Losartan potassium Tablets, 100 mg 67046-1511-03 Coupler 30 tablets AB FDA listed
LOSARTAN POTASSIUM 100 mg 68071-2203-09 NuCare 90 tablets AB FDA listed
Losartan Potassium 100 mg 68071-2344-03 NuCare 30 tablets AB FDA listed
Losartan potassium 100 mg 70518-4289-00 REMEDYREPACK 30 tablets AB FDA listed
Losartan potassium Tablets, 100 mg 72162-1698-00 Bryant 1000 tablets AB FDA listed
Losartan Potassium 100 mg 72162-2508-00 Bryant 1000 tablets AB FDA listed
Losartan Potassium 100 mg 65841-0731-01 Zydus 100 tablets AB FDA listed
Losartan Potassium 100 mg 46708-0447-30 Alembic 30 tablets AB FDA listed
Losartan Potassium 100 mg 50090-4914-00 A-S 90 tablets AB FDA listed
Losartan Potassium 100 mg 51655-0791-26 Northwind 90 tablets AB FDA listed
Losartan Potassium 100 mg 68071-5181-09 NuCare 90 tablets AB FDA listed
Losartan potassium Tablets, 100 mg 59746-0335-01 Jubilant 100 tablets AB FDA listed
Losartan Potassium 100 mg 68071-2216-03 NuCare 30 tablets AB FDA listed
Losartan Potassium 100 mg 68788-8186-01 Preferred 100 tablets AB FDA listed
Losartan Potassium 100 mg 71335-1580-01 Bryant 30 tablets AB FDA listed
Losartan Potassium 100 mg 72189-0097-30 Direct_Rx 30 tablets AB FDA listed
Losartan Potassium 100 mg 72789-0044-30 PD-Rx 30 tablets AB FDA listed
Losartan Potassium 100 mg 31722-0702-05 Camber 500 tablets AB FDA listed
Losartan Potassium 100 mg 67046-0702-03 Coupler 30 tablets AB FDA listed
Losartan Potassium 100 mg 70518-0718-00 REMEDYREPACK 30 tablets AB FDA listed
Losartan Potassium 100 mg 55154-6643-00 Cardinal 1 tablet AB FDA listed
Losartan Potassium 100 mg 68382-0137-01 Zydus 100 tablets AB FDA listed
Losartan Potassium 100 mg 71335-2083-01 Bryant 30 tablets AB FDA listed
Losartan Potassium 100 mg 70518-4695-00 REMEDYREPACK 100 tablets AB FDA listed
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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

🏛️
1995
On the market since
Apr 1995
📍
2026
Currently FDA-listed
31 years listed
🔓
·
Generic versions listed
see equivalents
Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Losartan Potassium (matched by generic name) — the program that covers self-administered drugs. 20 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Losartan Potassium. CMS lists 3 products for this generic; we show the highest-spend one. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$87.55M
Claims incl. refills
9.7M
Beneficiaries
7.6M
Spend / beneficiary
$11.46
Spend / claim
$8.99
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

🔬 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 Losartan Potassium — the ingredient across all brands.

Top reported reactions

Fatigue6,464
Nausea5,301
Diarrhoea5,184
Dyspnoea4,689
Dizziness4,429
Headache4,285
Pain3,907

Age at onset

Neonate11
Infant5
Child7
Adolescent11
Adult6,203
Elderly8,653

Reporter sex

89,498 reports
Male · 39%
Female · 61%
Unknown · 0%

Serious outcomes

Hospitalization27,390
Life-threatening2,808
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 5,928 3,120
Most recent year is provisional (FAERS lags ~3 months).
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
60312-0960-00 You're viewing this 1 BAG in 1 DRUM (60312-0960-0) / 97000 TABLET, FILM COATED in 1 BAG Active

🧭 About this NDC listing & data coverage

Listed for further processing / repackaging

What "drug for further processing" means

FDA lists this package under the "drug for further processing" marketing category: ORGANON PHARMA (UK) LIMITED supplies it to other companies for further processing or repackaging (blister cards that are later repackaged or co-packaged are a common example). The units themselves are a finished dosage form — which is why pricing or Medicaid data can still appear — but this exact package code may not be the presentation a retail pharmacy dispenses.

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 — Not published for this NDC No photo available yet for this listing.
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

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Drug For Further Processing". Products approved under an application carry an NDA, ANDA, or BLA number.
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.
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 FDA registers it as 60312-0960-0, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 60312-0960-00, written without dashes as 60312096000. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 60312-0960-00, the first segment (60312) is the labeler code FDA assigned to ORGANON PHARMA (UK) LIMITED; the middle segment (0960) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by ORGANON PHARMA (UK) LIMITED. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
ORGANON PHARMA (UK) LIMITED 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.
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.

📄 Full FDA label FDA SPL

The complete FDA label for this product, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label 19 words

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

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