NDC 67046-1536 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67046-1536

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Coupler LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
March 25, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
67046-1536-330 TABLET in 1 BLISTER PACK (67046-1536-3)Mar 25, 2025

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