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⚪no package photo
in the FDA label

Pravastatin Sodium 10 mg Tablet, 1,000-count

by AvKARE · 1000 TABLET in 1 BOTTLE (42291-665-10)
NDC 42291-0665-10
🏷️ FDA NDC (as labeled) 42291-665-10 billing pads the product segment with a zero
This package
Contains1,000-count Pack sizes2 compare ↓
Also comes in: 90 tablets 42291-0665-90
Rx only Generic Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Mar 13, 2024 · 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

⚠️
Other active recalls for Pravastatin Sodium (different manufacturers) — 5 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 13, 2025 — CGMP Deviations (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0350-2025
Class II · Mar 13, 2025 — CGMP Deviations (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0341-2025
Class II · Mar 13, 2025 — CGMP Deviations (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0349-2025
Class II · Mar 13, 2025 — CGMP Deviations (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0325-2025
Class II · Jun 28, 2024 — Failed Dissolution Specifications: results below specifications (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0612-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Nov 2025. 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

FDA NDC (as labeled) 42291-665-10
Product NDC 42291-665
11-digit billing NDC 42291066510
NCPDP billing unit EA — each (per item)
Application # ANDA076056
Mechanism of action HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors
DEA schedule Non-controlled
Marketing category ANDA
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Nov 2025)
Route ORAL
Dosage form TABLET
Substance PRAVASTATIN SODIUM
GCN Seq No 016366
GCN 48671
HICL code 006227
Ingredient (HICL) Pravastatin Sodium
HIC1 code M
Therapeutic class — broad (HIC1) Blood
HIC2 code M4
Therapeutic class — intermediate (HIC2) Affect Blood Lipids/Sugar/Amino Acids
HIC3 code M4D
Therapeutic class — specific (HIC3) Antihyperlipidemic-Hmgcoa Reductase Inhib(Statins)
AHFS code 24:06.08.00
AHFS class Hmg-Coa Reductase Inhibitors
FDB label name PRAVASTATIN SODIUM 10 MG TAB
FDB brand name Pravastatin Sodium
Legend status F — Federal legend — prescription drug or device
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 42291-665-10 — 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 → 42291-0665-10. 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

LabelerAvKARE
Application holderAUROBINDO PHARMA USA INC
FDA applicationANDA076056 (ANDA)
Labeler code42291
Product typeHuman Prescription Drug
Portfolio384 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

Label name PRAVASTATIN SODIUM 10 MG TAB Ingredient Pravastatin Sodium
📖 What it is MedlinePlus · NLM

Pravastatin is used to reduce the risk of heart attack and stroke decrease the amount of cholesterol (a fat-like substance that can build up and clog blood vessels causing heart attack or stroke or other health conditions) Pravastatin is in a class of medications called HMG-CoA reductase inhibitors (statins). It works by slowing how much cholesterol your body makes. This lowers the amount of cholesterol that can build up on the walls of the arteries and block blood flow to the heart, brain, and other parts of the body.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Pravastatin works in two main ways. First, it lowers your LDL (bad cholesterol) and triglycerides while nudging your HDL (good cholesterol) higher. Second — and this is the big one...
  • What exactly is pravastatin supposed to do for me?
  • Good news — pravastatin is flexible. You can take it at any time of day, morning or evening, and with or without food. The cholesterol-lowering effect is similar either way. The on...
  • Does it matter what time of day I take it, or whether I take it with food?
📖 Read our full Pravastatin guide →
1
Nutrient depletion considerations

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

🧪 Full Pravastatin Sodium nutrient depletion report →
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.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
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.
Try another pack size: 90 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Pravastatin Sodium 10 mg 00093-0771-10 Teva 1000 tablets $0.057 AB Availability likely —
Pravastatin Sodium 10 mg 00904-5891-61 Major 100 tablets $0.057 AB Availability likely —
Pravastatin Sodium 10 mg 16714-0558-01 NorthStar 90 tablets $0.057 AB Availability likely —
Pravastatin Sodium 10 mg 50268-0665-15 AvPAK 50 tablets $0.057 AB Availability likely —
Pravastatin Sodium 10 mg 60687-0886-01 American 100 tablets $0.057 AB Availability likely —
Pravastatin Sodium 10 mg 68462-0195-05 Glenmark 500 tablets $0.057 AB Availability likely —
Pravastatin Sodium 10 mg 69097-0788-05 CIPLA 90 tablets $0.057 AB Availability likely —
Pravastatin sodium 10 mg 84386-0031-90 Aurobindo 90 tablets $0.057 AB Availability likely —
Pravastatin Sodium 10 mg 16729-0008-15 Accord 90 tablets $0.058 AB FDA listed —
Pravastatin Sodium 10 mg 00615-8539-39 NCS 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 00615-8618-39 NCS 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 50090-1594-00 A-S 90 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 50090-3853-00 A-S 90 tablets — AB FDA listed —
Pravastatin sodium 10 mg 51407-0887-10 Golden 1000 tablets — AB FDA listed —
Pravastatin sodium 10 mg 55111-0229-01 Dr.Reddy's 100 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 55154-3350-00 Cardinal 10 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 60505-0168-01 Apotex 100 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 62135-0847-90 Chartwell 90 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 63629-8833-01 Bryant 90 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 63629-8904-01 Bryant 90 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 63629-8905-01 Bryant 1000 tablets — AB Discontinued —
Pravastatin Sodium 10 mg 63629-9162-01 Bryant 30 tablets — AB FDA listed —
Pravastatin sodium 10 mg 65862-0632-05 Aurobindo 500 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 67046-1518-03 Coupler 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 67046-1621-03 Coupler 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 68071-5001-03 NuCare 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 68071-5007-03 NuCare 30 tablets — AB FDA listed —
Pravastatin sodium 10 mg 68788-4059-03 Preferred 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 68788-8425-03 Preferred 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 69292-0101-10 Amici 1000 tablets — AB FDA listed —
Pravastatin sodium 10 mg 70377-0045-11 Biocon 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 70518-0549-00 REMEDYREPACK 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 71335-1243-01 Bryant 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 71335-2298-01 Bryant 1000 tablets — AB FDA listed —
Pravastatin sodium 10 mg 71335-2848-01 Bryant 90 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 72162-1706-03 Bryant 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 72162-1951-00 Bryant 1000 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 72189-0059-90 DIRECT 90 tablets — AB FDA listed —
Pravastatin Sodium 10 mg 82868-0104-30 Northwind 30 tablets — AB FDA listed —
Pravastatin Sodium 10 mgthis 42291-0665-10 AvKARE 1000 tablets — AB 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

📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
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.

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

Medicare Part D (outpatient prescription) spending for Pravastatin Sodium — the program that covers self-administered drugs. 14 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 Pravastatin Sodium. 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
$31.8M
Claims incl. refills
2.1M
Beneficiaries
1.7M
Spend / beneficiary
$18.70
Spend / claim
$15.06
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
42291-0665-10 You're viewing this 1000 TABLET in 1 BOTTLE (42291-665-10) 2014-06-30 Discontinued by firm
42291-0665-90 90 TABLET in 1 BOTTLE (42291-665-90) 2014-06-30 Discontinued by firm

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 42291-0665-10?
NDC 42291-0665-10 is a 1,000-count package — 1000 tablet in 1 bottle.
What is the difference between NDC 42291-0665-10 and NDC 42291-0665-90?
Both are Pravastatin Sodium 10 mg Tablet — the drug itself is identical. NDC 42291-0665-10 is the 1,000-count package, while NDC 42291-0665-90 is the 90 tablets package.
What NDC number is used to bill for this package of Pravastatin Sodium 10 mg Tablet?
Bill NDC 42291-0665-10 — the 11-digit billing format is 42291066510. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Finished prescription 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) — Not published for this NDC No structured label is linked to this listing in DailyMed/openFDA.
Package photos — Not published for this NDC The FDA label for this product carries no photos.
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 ✓ Available
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.
Why is there no full label on this page?
No structured FDA label (SPL) is currently linked to this NDC in DailyMed/openFDA. That can happen with older listings, certain OTC and repackaged products, and recently updated listings whose label has not yet propagated. The listing itself is still valid — this page shows everything the public feeds provide for this package.
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 FDA registers it as 42291-665-10, 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: 42291-0665-10, written without dashes as 42291066510. 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 42291-0665-10, the first segment (42291) is the labeler code FDA assigned to AvKARE; the middle segment (0665) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (10) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 90 tablets (42291-0665-90). 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?
AvKARE 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 a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
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 prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label
📄 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.
← 42291-0664-10 · AvKARE 42291-0666-10 · AvKARE →
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.