NDC 71335-1007 – Gabapentin

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

Human Prescription Drug

Product NDC71335-1007

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 (9)

Package NDCDescriptionSince
71335-1007-130 TABLET, FILM COATED in 1 BOTTLE (71335-1007-1)Aug 1, 2019
71335-1007-260 TABLET, FILM COATED in 1 BOTTLE (71335-1007-2)Nov 14, 2018
71335-1007-390 TABLET, FILM COATED in 1 BOTTLE (71335-1007-3)Nov 14, 2018
71335-1007-4180 TABLET, FILM COATED in 1 BOTTLE (71335-1007-4)Apr 9, 2024
71335-1007-5120 TABLET, FILM COATED in 1 BOTTLE (71335-1007-5)Jan 28, 2019
71335-1007-6100 TABLET, FILM COATED in 1 BOTTLE (71335-1007-6)Apr 9, 2024
71335-1007-784 TABLET, FILM COATED in 1 BOTTLE (71335-1007-7)Apr 9, 2024
71335-1007-8112 TABLET, FILM COATED in 1 BOTTLE (71335-1007-8)Apr 9, 2024
71335-1007-9135 TABLET, FILM COATED in 1 BOTTLE (71335-1007-9)Apr 9, 2024

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