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
- 68382-205_e85a763f-472b-492b-bf25-a30251b9b50b
- Product NDC
- 68382-205
- Form
- TABLET, FILM COATED
- Composition / generic term
- Gabapentin
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121016
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (68382-205-01) · 68382-205-01
- 500 TABLET, FILM COATED in 1 BOTTLE (68382-205-05) · 68382-205-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (68382-205-10) · 68382-205-10
- 100 BLISTER PACK in 1 CARTON (68382-205-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-205-30) · 68382-205-77
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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