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Ranolazine 1000 mg Tablet, Film Coated, Extended Release, 800-count — NDC 59651-010-82 (Billing 59651-0010-82)

by Aurobindo Pharma Limited · 800 TABLET, FILM COATED, EXTENDED RELEASE in 1 BAG

This is a package of 800 tablets of Ranolazine 1000 mg Tablet, Film Coated, Extended Release from Aurobindo Pharma Limited, marketed since Dec 2022 and currently FDA-listed.

NDC 59651-0010-82
🏷️ FDA NDC (as labeled) 59651-010-82 billing pads the product segment with a zero
This package
Contains800-count Pack sizes4 compare ↓
Product page 59651-0010-60 Also comes in: 60 tablets 59651-010-60 180 tablets 59651-010-18 1000 tablets 59651-010-99
On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 8, 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

NDC database record

One package, one record: these facts belong to NDC 59651-010-82 alone.

Record
FDA NDC Directory package listing · Drug for further processing
Code segments
59651 labeler · 010 product · 82 package
Package marketed since
Dec 23, 2022
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 5965101082 2
FDA record last changed
Oct 8, 2026
⚠️
Other active recalls for Ranolazine (different manufacturers) — 2 · 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-0335-2025
Class II · Oct 23, 2023 — Failed Dissolution Specifications: Out of specification for dissolution. (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0092-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 59651-010-82
Product NDC 59651-010
11-digit billing NDC 59651001082
SPL Set ID 69590941-6ede-457f-8504-4e8581bc06b2
DEA schedule Non-controlled
Marketing category DRUG FOR FURTHER PROCESSING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-12-23
Dosage form TABLET, FILM COATED, EXTENDED RELEASE
Substance RANOLAZINE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 32200040007430
GCN Seq No 062973
GCN 98733
HICL code 033446
Ingredient (HICL) Ranolazine
HIC1 code A
Therapeutic class — broad (HIC1) Cardiovascular System
HIC2 code A2
Therapeutic class — intermediate (HIC2) Cardiac Depressants
HIC3 code A2C
Therapeutic class — specific (HIC3) Antianginal, Anti-Ischemic Agents,Non-Hemodynamic
AHFS code 24:04.92.00
AHFS class Cardiac Drugs, Miscellaneous
FDB label name RANOLAZINE ER 1,000 MG TABLET
FDB brand name Ranolazine Er
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 062973
  • GCN: 98733
  • GPI-14 (Medi-Span): 32200040007430
  • HICL (First Databank): 033446
  • AHFS class code: 24:04.92.00
Why two NDCs? The FDA registers this code as 59651-010-82 — 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 → 59651-0010-82. 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.

Clinical

Label name RANOLAZINE ER 1,000 MG TABLET Ingredient Ranolazine
📖 What it is MedlinePlus · NLM

Ranolazine is used alone or with other medications to treat chronic angina (ongoing chest pain or pressure that is felt when the heart does not get enough oxygen). Ranolazine is in a class of medications called anti-anginals. The exact way that ranolazine works is not known at this time.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • It treats chronic angina, which is recurring chest pain from reduced blood flow to the heart. You can take it along with other heart medicines such as beta-blockers or nitrates. It...
  • Take it by mouth twice a day, as your prescriber directs. Extended-release tablets can be taken with or without food and must be swallowed whole. Aspruzyo Sprinkle granules go on a...
  • The most common are dizziness, headache, constipation, and nausea. Tell me or your doctor if they bother you. Call right away if you faint, have a pounding or irregular heartbeat,...
  • Many medicines interact with it, so always check with me first. Some, like ketoconazole, clarithromycin, rifampin, and St. John’s wort, must not be used at all. Others, like diltia...
📖 Read our full Ranolazine guide →
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: 60 tablets 180 tablets 1000 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 Per unit Per pack Marketing startMarketing endStatus
59651-0010-18 59651-010-18 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE — — 2022-12-23 — Active
59651-0010-60 59651-010-60 Main listing 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE $0.2743 / ea $16.46 2022-12-23 — Active
59651-0010-99 59651-010-99 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE — — 2022-12-23 — Active
59651-0010-82 You're viewing this 800 TABLET, FILM COATED, EXTENDED RELEASE in 1 BAG — — — — Active

You're viewing one of 4 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 800-count package — 800 tablet, film coated, extended release in 1 bag.
How does this package differ from NDC 59651-0010-60?
Both are Ranolazine 1000 mg Tablet, Film Coated, Extended Release — the drug itself is identical. This page's package is the 800-count one, while NDC 59651-0010-60 is the 60 tablets package.
What NDC number is used to bill for this package of Ranolazine 1000 mg Tablet, Film Coated, Extended Release?
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.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Ranolazine 1000 mg 27241-0126-02 Ajanta 60 tablets $0.274 AB Availability likely —
Ranolazine 1000 mg 31722-0669-60 Camber 60 tablets $0.274 AB Availability likely —
Ranolazine 1000 mg 50268-0723-13 AvPAK 1 tablet $0.274 AB Availability likely —
Ranolazine 1000 mg 69367-0294-60 Westminster 60 tablets $0.274 AB Availability likely —
Ranolazine 1000 mg 70756-0704-60 Lifestar 60 tablets $0.274 AB Availability likely —
Ranolazine 1000 mg 72319-0022-02 i3 60 tablets $0.274 AB Availability likely —
Ranolazine 1000 mg 90096-0152-60 Zameer 60 tablets $0.274 AB Availability likely —
Ranolazine 1000 mg 13668-0760-60 Torrent 60 tablets — AB FDA listed —
Ranolazine 1000 mg 29300-0297-01 Unichem 100 tablets — AB FDA listed —
Ranolazine 1000 mg 42291-0774-60 AvKARE 60 tablets — AB FDA listed —
Ranolazine 1000 mg 42571-0325-11 Micro 10 tablets — — Discontinued —
Ranolazine 1000 mg 50228-0424-05 ScieGen 500 tablets — AB FDA listed —
Ranolazine 1000 mgthis 59651-0010-82 Aurobindo 800 tablets — — FDA listed —
Ranolazine 1000 mg 63304-0018-05 Sun 500 tablets — — FDA listed —
Ranolazine 1000 mg 67877-0526-05 Ascend 500 tablets — AB FDA listed —
Ranolazine 1000 mg 68462-0320-05 Glenmark 500 tablets — AB FDA listed —
Ranolazine 1000 mg 70625-0207-01 SunGen 60 tablets — AB FDA listed —
Ranolazine 1000 mg 70771-1500-01 Zydus 100 tablets — AB FDA listed —
Ranolazine 1000 mg 71205-0868-00 Proficient 100 tablets — AB FDA listed —
Ranolazine 1000 mg 72578-0065-01 Viona 100 tablets — AB FDA listed —
Ranolazine 1000 mg 73141-0022-02 A2A 60 tablets — AB FDA listed —
Ranolazine 1000 mg 77771-0424-60 Radha 60 tablets — AB FDA listed —
Ranolazine 1000 mg 68180-0355-02 Lupin 500 tablets — AB FDA listed —
Ranolazine 1000 mg 60290-0056-01 Umedica 60 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

🏛️
2022
On the market since
Dec 2022
📍
2026
Currently FDA-listed
4 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.

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.

🧪 Avoiding an ingredient? See Ranolazine inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

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

LabelerAurobindo Pharma Limited
Labeler code59651
First marketedDec 2022
Product typeDrug For Further Processing
Portfolio1,464 products on file

More NDCs from Aurobindo Pharma Limited labeler code 59651

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.

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
📄 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 ↗

Medicaid utilization by pack size

Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
60 tablets59651-0010-60 30 Rx · $937
180 tablets59651-0010-18 No Medicaid data
1000 tablets59651-0010-99 No Medicaid data
800 tablets this page59651-0010-82 No Medicaid data
Drug total (last 4 qtrs): 30 Rx · 2,040 units · $937 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.

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

Medicare Part D (outpatient prescription) spending for Ranolazine ER (matched by generic name) — the program that covers self-administered drugs. 16 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 Ranolazine ER. 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
$22.88M
Claims incl. refills
332.4K
Beneficiaries
221.5K
Spend / beneficiary
$103.31
Spend / claim
$68.83
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.

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: Aurobindo Pharma 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 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.
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 Aurobindo Pharma Limited. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 60 tablets (59651-0010-60), 180 tablets (59651-0010-18), 1000 tablets (59651-0010-99). 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?
Aurobindo Pharma 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.
← 59651-0009-18 · Aurobindo 59651-0011-37 · Aurobindo →
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.