NDC 71335-1132 – Gabapentin

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

Human Prescription Drug

Product NDC71335-1132

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 (10)

Package NDCDescriptionSince
71335-1132-028 TABLET, FILM COATED in 1 BOTTLE (71335-1132-0)Apr 2, 2024
71335-1132-130 TABLET, FILM COATED in 1 BOTTLE (71335-1132-1)Sep 18, 2019
71335-1132-260 TABLET, FILM COATED in 1 BOTTLE (71335-1132-2)Mar 22, 2019
71335-1132-3180 TABLET, FILM COATED in 1 BOTTLE (71335-1132-3)Mar 24, 2020
71335-1132-490 TABLET, FILM COATED in 1 BOTTLE (71335-1132-4)Mar 21, 2019
71335-1132-5100 TABLET, FILM COATED in 1 BOTTLE (71335-1132-5)Apr 2, 2024
71335-1132-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1132-6)Apr 5, 2019
71335-1132-7500 TABLET, FILM COATED in 1 BOTTLE (71335-1132-7)Apr 2, 2024
71335-1132-884 TABLET, FILM COATED in 1 BOTTLE (71335-1132-8)Apr 2, 2024
71335-1132-9112 TABLET, FILM COATED in 1 BOTTLE (71335-1132-9)Apr 2, 2024

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