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Gabapentin 400 mg Capsule, 120-count — NDC 87063-686-12 (Billing 87063-0686-12)

by ASCLEMED USA INC. · 120 CAPSULE in 1 BOTTLE

This is a package of 120 capsules of Gabapentin 400 mg Capsule from ASCLEMED USA INC., marketed since Jan 2011 and currently FDA-listed. It is the main listing for this product, which comes in 4 package sizes.

NDC 87063-0686-12
🏷️ FDA NDC (as labeled) 87063-686-12 billing pads the product segment with a zero
This package
Contains120-count Pack sizes4 compare ↓
Main listing for product 87063-686 · Also comes in: 30 capsules 87063-686-30 60 capsules 87063-686-60 90 capsules 87063-686-90
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

⚠️
Other active recalls for Gabapentin (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 10, 2025 — Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity . (The Harvard Drug Group LLC) · FDA recall D-0031-2026
Class II · Oct 10, 2025 — Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity . (The Harvard Drug Group LLC) · FDA recall D-0030-2026
Class II · Jun 19, 2025 — Defective container; blister packaging inadequately sealed. (The Harvard Drug Group LLC) · FDA recall D-0507-2025
Class II · Jun 19, 2025 — Defective container; blister packaging inadequately sealed. (The Harvard Drug Group LLC) · FDA recall D-0508-2025
Class II · Mar 13, 2025 — CGMP Deviations (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0320-2025
Class III · Mar 4, 2025 — Cross Contamination (SUN PHARMACEUTICAL INDUSTRIES INC) · FDA recall D-0312-2025
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) 87063-686-12
Product NDC 87063-686
11-digit billing NDC 87063068612
Application # ANDA090858
SPL Set ID 55115803-fea0-5de5-e063-6294a90a9f03
Physiologic effect Decreased Central Nervous System Disorganized Electrical Activity
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-01-29
Route ORAL
Dosage form CAPSULE
Substance GABAPENTIN
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 87063-686-12 — 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 → 87063-0686-12. 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

📗 Our plain-language guide HelloPharmacist
  • It's used for nerve pain after shingles (postherpetic neuralgia). Many gabapentin products are also used as add-on treatment for partial seizures in epilepsy. Horizant is also used...
  • Dizziness and sleepiness are the most common side effects. Don't drive or use heavy machinery until you know how it affects you, because you may not judge your own impairment well.
  • Talk to your prescriber first. Stopping seizure medicines suddenly can increase seizures. Gralise should be changed or stopped gradually over at least a week.
  • Tell me about any opioid or sedating medicine, because together they can slow breathing dangerously. If you use an antacid like Maalox, take gabapentin at least 2 hours after it.
📖 Read our full Gabapentin guide →
1
Nutrient depletion considerations

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

🧪 Full Gabapentin 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.

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: 30 capsules 60 capsules 90 capsules
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
87063-0686-12 You're viewing this Main listing 120 CAPSULE in 1 BOTTLE 2026-06-25 — Active
87063-0686-30 87063-686-30 30 CAPSULE in 1 BOTTLE 2026-06-25 — Active
87063-0686-60 87063-686-60 60 CAPSULE in 1 BOTTLE 2026-06-25 — Active
87063-0686-90 87063-686-90 90 CAPSULE in 1 BOTTLE 2026-06-25 — Active

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

Pack size FAQ

What quantity is in this package?
This is a 120-count package — 120 capsule in 1 bottle.
How does this package differ from NDC 87063-0686-30?
Both are Gabapentin 400 mg Capsule — the drug itself is identical. This page's package is the 120-count one, while NDC 87063-0686-30 is the 30 capsules package.
What NDC number is used to bill for this package of Gabapentin 400 mg Capsule?
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
Gabapentin 400 mg 63739-0904-10 McKesson 100 capsules $0.041 AB Availability likely —
Gabapentin 400 mg 70010-0118-01 Granules 100 capsules $0.042 AB Discontinued —
Gabapentin 400 mg 71093-0122-04 ACI 100 capsules $0.042 AB Discontinued —
Gabapentin 400 mg 45963-0557-11 Actavis 100 capsules $0.042 AB Availability likely —
Relgaabi 400 mg 58657-0234-01 Method 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 69367-0133-06 Westminster 500 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 50228-0181-01 ScieGen 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 69367-0345-05 Westminster 500 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 49483-0607-01 TIME 100 capsules $0.042 AB Availability likely —
gabapentin 400 mg 16571-0869-01 Rising 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 31722-0150-01 Camber 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 69097-0815-07 Cipla 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 00904-6667-61 Major 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 00904-7615-61 Major 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 65862-0200-01 Aurobindo 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 16714-0663-01 NorthStar 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 64380-0731-01 Strides 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 23155-0868-01 Heritage 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 60687-0602-01 American 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 69292-0642-01 Amici 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 67877-0224-01 Ascend 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 70010-0928-01 Granules 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 83301-0005-01 Mullan 100 capsules $0.042 AB Availability likely —
Gabapentin 400 mg 64380-0869-06 Strides 100 capsules $0.052 AB FDA listed —
Neurontin 400 mg 58151-0283-01 Viatris 100 capsules $8.867 AB Availability likely —
Neurontin 400 mg 00071-0806-24 Parke-Davis 100 capsules $8.867 AB Discontinued —
Gabapentin 400 mg 42582-0116-10 Bi-Coastal 100 capsules — AB FDA listed —
Gabapentin 400 mg 42806-0511-01 Epic 100 capsules — AB FDA listed —
Gabapentin 400 mg 43353-0081-60 Aphena 90 capsules — AB FDA listed —
Gabapentin 400 mg 63187-0909-00 Proficient 100 capsules — AB FDA listed —
Gabapentin 400 mg 71205-0064-30 Proficient 30 capsules — AB FDA listed —
Gabapentin 400 mg 71205-0485-30 Proficient 30 capsules — AB FDA listed —
Gabapentin 400 mg 71205-0619-30 Proficient 30 capsules — AB FDA listed —
Gabapentin 400 mg 71205-0930-00 Proficient 100 capsules — AB FDA listed —
Gabapentin 400 mg 71610-0059-60 Aphena 90 capsules — AB FDA listed —
Gabapentin 400 mg 71610-0166-60 Aphena 90 capsules — AB FDA listed —
Gabapentin 400 mg 76420-0234-12 Asclemed 120 capsules — AB FDA listed —
Gabapentin 400 mg 53746-0103-01 Amneal 100 capsules — AB FDA listed —
Gabapentin 400 mg 71205-0671-30 Proficient 30 capsules — AB FDA listed —
Gabapentin 400 mg 71205-0808-30 Proficient 30 capsules — AB FDA listed —
Gabapentin 400 mg 71610-0757-53 Aphena 60 capsules — AB FDA listed —
Gabapentin 400 mg 72162-2140-01 Bryant 100 capsules — AB FDA listed —
Gabapentin 400 mg 76420-0790-01 Asclemed 100 capsules — AB FDA listed —
Gabapentin 400 mg 58118-1103-08 Clinical 30 capsules — AB FDA listed —
Gabapentin 400 mg 63629-8488-01 Bryant 100 capsules — AB FDA listed —
Gabapentin 400 mg 82619-0144-01 Creekwood 100 capsules — AB FDA listed —
Gabapentin 400 mg 50090-1072-00 A-S 90 capsules — AB FDA listed —
Gabapentin 400 mg 71335-2700-00 Bryant 180 capsules — AB FDA listed —
Gabapentin 400 mg 72189-0524-90 Direct_Rx 90 capsules — AB FDA listed —
Gabapentin 400 mg 72737-0007-01 STALLION 30 capsules — AB FDA listed —
gabapentin 400 mg 70518-4482-00 REMEDYREPACK 90 capsules — AB FDA listed —
Gabapentin 400 mg 71335-1199-00 Bryant 180 capsules — AB Discontinued —
Gabapentin 400 mg 71335-1496-01 Bryant 90 capsules — AB Discontinued —
Gabapentin 400 mg 71335-2773-01 Bryant 90 capsules — AB FDA listed —
Gabapentin 400 mg 71610-0631-53 Aphena 60 capsules — AB FDA listed —
Gabapentin 400 mg 69434-0044-03 Zhejiang 500 capsules — AB FDA listed —
Gabapentin 400 mg 71335-0820-01 Bryant 90 capsules — AB FDA listed —
Gabapentin 400 mg 72865-0254-05 XLCare 500 capsules — AB FDA listed —
gabapentin 400 mg 82804-0294-90 Proficient 90 capsules — AB FDA listed —
Gabapentin 400 mg 55700-0812-30 Quality 30 capsules — AB Discontinued —
Gabapentin 400 mg 71335-0351-00 Bryant 180 capsules — AB FDA listed —
Gabapentin 400 mg 71335-2381-01 Bryant 90 capsules — AB FDA listed —
Gabapentin 400 mg 72162-1534-01 Bryant 100 capsules — AB FDA listed —
Gabapentin 400 mg 80425-0082-03 Advanced 90 capsules — AB FDA listed —
Gabapentin 400 mg 80425-0163-03 Advanced 90 capsules — AB FDA listed —
Gabapentin 400 mg 80425-0286-01 Advanced 30 capsules — AB FDA listed —
Gabapentin 400 mg 83008-0049-60 Quality 60 capsules — AB Discontinued —
Gabapentin 400 mg 83209-0663-30 Boswell 30 capsules — AB FDA listed —
Gabapentin 400 mg 42385-0974-01 Laurus 100 capsules — AB FDA listed —
Gabapentin 400 mg 43547-0481-10 Solco 100 capsules — AB FDA listed —
gabapentin 400 mg 67046-1591-03 Coupler 30 capsules — AB FDA listed —
Gabapentin 400 mg 68788-8816-01 Preferred 100 capsules — AB FDA listed —
Gabapentin 400 mg 70518-1469-00 REMEDYREPACK 30 capsules — AB FDA listed —
Gabapentin 400 mg 76420-0870-01 Asclemed 100 capsules — AB FDA listed —
Gabapentin 400 mg 51407-0049-05 Golden 500 capsules — AB Discontinued —
Gabapentin 400 mg 60760-0846-30 St. 30 capsules — AB FDA listed —
gabapentin 400 mg 62756-0139-01 Sun 50 capsules — — FDA listed —
Gabapentin 400 mg 25000-0105-03 MARKSANS 30 capsules — AB FDA listed —
Gabapentin 400 mg 58118-3224-08 Clinical 30 capsules — AB FDA listed —
Gabapentin 400 mg 60760-0864-90 ST. 90 capsules — AB Discontinued —
Gabapentin 400 mg 71610-0198-53 Aphena 60 capsules — AB FDA listed —
Gabapentin 400 mg 72189-0113-30 DIRECT 30 capsules — AB FDA listed —
Gabapentin 400 mg 65162-0103-03 Amneal 30 capsules — AB FDA listed —
Gabapentin 400 mg 68788-7838-01 Preferred 100 capsules — AB FDA listed —
Gabapentin 400 mg 71335-2478-00 Bryant 180 capsules — AB FDA listed —
Gabapentin 400 mg 76282-0323-01 Exelan 100 capsules — AB FDA listed —
Gabapentin 400 mg 55154-7993-00 Cardinal 10 capsules — AB FDA listed —
Gabapentin 400 mg 70518-2919-01 REMEDYREPACK 30 capsules — AB FDA listed —
Gabapentin 400 mg 71335-0214-00 Bryant 180 capsules — AB FDA listed —
Gabapentin 400 mg 85534-0008-00 HAWAII 30 capsules — AB FDA listed —
Gabapentin 400 mgthis 87063-0686-12 ASCLEMED 120 capsules — AB FDA listed —
Gabapentin 400 mg 00480-3496-77 Teva 15920 capsules — AB FDA listed —
Gabapentin 400 mg 70518-0053-00 REMEDYREPACK 30 capsules — AB FDA listed —
Gabapentin 400 mg 55154-0579-00 Cardinal 10 capsules — AB FDA listed —
Gabapentin 400 mg 70518-4740-00 REMEDYREPACK 30 capsules — AB FDA listed —
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

🏛️
2011
On the market since
Jan 2011
📍
2026
Currently FDA-listed
15 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.

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.

Manufacturer & labeler

LabelerASCLEMED USA INC.
Application holderALKEM LABORATORIES LTD
FDA applicationANDA090858 (ANDA)
Labeler code87063
First marketedJan 2011
Product typeHuman Prescription Drug
Portfolio129 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.

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. Prefer the government’s original formatting? View this label on DailyMed ↗

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

Medicare Part D (outpatient prescription) spending for Gabapentin — the program that covers self-administered drugs. 41 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 Gabapentin. 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
$151.2M
Claims incl. refills
8.9M
Beneficiaries
5.1M
Spend / beneficiary
$29.73
Spend / claim
$16.90
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

Finished prescription product
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 ✓ 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.
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 ASCLEMED USA INC.. 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 30 capsules (87063-0686-30), 60 capsules (87063-0686-60), 90 capsules (87063-0686-90). 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?
ASCLEMED USA INC. 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.
← 87063-0309-01 · ASCLEMED 87063-0687-12 · ASCLEMED →
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.