NDC 71335-2765 – Gabapentin

Gabapentin 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2765

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200651
Marketed since
October 6, 2011
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (9)

Package NDCDescriptionSince
71335-2765-130 TABLET, FILM COATED in 1 BOTTLE (71335-2765-1)Oct 3, 2025
71335-2765-260 TABLET, FILM COATED in 1 BOTTLE (71335-2765-2)Oct 3, 2025
71335-2765-390 TABLET, FILM COATED in 1 BOTTLE (71335-2765-3)Oct 3, 2025
71335-2765-4180 TABLET, FILM COATED in 1 BOTTLE (71335-2765-4)Oct 3, 2025
71335-2765-5120 TABLET, FILM COATED in 1 BOTTLE (71335-2765-5)Oct 3, 2025
71335-2765-6100 TABLET, FILM COATED in 1 BOTTLE (71335-2765-6)Oct 3, 2025
71335-2765-784 TABLET, FILM COATED in 1 BOTTLE (71335-2765-7)Oct 3, 2025
71335-2765-8112 TABLET, FILM COATED in 1 BOTTLE (71335-2765-8)Oct 3, 2025
71335-2765-9135 TABLET, FILM COATED in 1 BOTTLE (71335-2765-9)Oct 3, 2025

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