United States · FDA National Drug Code directory
Gabapentin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 76420-497_eaa81374-5d2c-60d1-e053-2a95a90af8ea
- Product NDC
- 76420-497
- Form
- TABLET
- Composition / generic term
- Gabapentin
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160204
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (76420-497-01) · 76420-497-01
- 500 TABLET in 1 BOTTLE (76420-497-05) · 76420-497-05
- 120 TABLET in 1 BOTTLE (76420-497-12) · 76420-497-12
- 240 TABLET in 1 BOTTLE (76420-497-24) · 76420-497-24
- 30 TABLET in 1 BOTTLE (76420-497-30) · 76420-497-30
- 60 TABLET in 1 BOTTLE (76420-497-60) · 76420-497-60
- 90 TABLET in 1 BOTTLE (76420-497-90) · 76420-497-90
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →