NDC 71335-1026 – Gabapentin

Gabapentin 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1026

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203244
Marketed since
January 11, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (6)

Package NDCDescriptionSince
71335-1026-190 TABLET, FILM COATED in 1 BOTTLE (71335-1026-1)Dec 13, 2018
71335-1026-258 TABLET, FILM COATED in 1 BOTTLE (71335-1026-2)Apr 2, 2024
71335-1026-3100 TABLET, FILM COATED in 1 BOTTLE (71335-1026-3)Sep 11, 2019
71335-1026-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1026-4)Mar 14, 2019
71335-1026-560 TABLET, FILM COATED in 1 BOTTLE (71335-1026-5)Jan 11, 2019
71335-1026-630 TABLET, FILM COATED in 1 BOTTLE (71335-1026-6)Jan 30, 2019

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