NDC 71335-1041 – Gabapentin

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

Human Prescription Drug

Product NDC71335-1041

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
71335-1041-190 TABLET, FILM COATED in 1 BOTTLE (71335-1041-1)Jan 29, 2019
71335-1041-218 TABLET, FILM COATED in 1 BOTTLE (71335-1041-2)Apr 2, 2024
71335-1041-358 TABLET, FILM COATED in 1 BOTTLE (71335-1041-3)Apr 2, 2024
71335-1041-460 TABLET, FILM COATED in 1 BOTTLE (71335-1041-4)Apr 28, 2020
71335-1041-530 TABLET, FILM COATED in 1 BOTTLE (71335-1041-5)Apr 8, 2019
71335-1041-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1041-6)Dec 27, 2018

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