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
- 70771-1862_ba40713a-2f22-4276-a664-355e7442cda4
- Product NDC
- 70771-1862
- Form
- TABLET
- Composition / generic term
- gabapentin
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240125
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (70771-1862-4) / 10 TABLET in 1 BLISTER PACK (70771-1862-2) · 70771-1862-4
- 500 TABLET in 1 BOTTLE (70771-1862-5) · 70771-1862-5
- 90 TABLET in 1 BOTTLE (70771-1862-9) · 70771-1862-9
Source and coverage
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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.
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