NDC 71335-1601 – Gabapentin

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

Human Prescription Drug

Product NDC71335-1601

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, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1601-130 TABLET, FILM COATED in 1 BOTTLE (71335-1601-1)Jun 18, 2020
71335-1601-260 TABLET, FILM COATED in 1 BOTTLE (71335-1601-2)Feb 14, 2022
71335-1601-390 TABLET, FILM COATED in 1 BOTTLE (71335-1601-3)Feb 14, 2022
71335-1601-4180 TABLET, FILM COATED in 1 BOTTLE (71335-1601-4)Feb 14, 2022
71335-1601-5120 TABLET, FILM COATED in 1 BOTTLE (71335-1601-5)Feb 14, 2022
71335-1601-6100 TABLET, FILM COATED in 1 BOTTLE (71335-1601-6)Feb 14, 2022
71335-1601-784 TABLET, FILM COATED in 1 BOTTLE (71335-1601-7)Feb 14, 2022
71335-1601-8112 TABLET, FILM COATED in 1 BOTTLE (71335-1601-8)Feb 14, 2022
71335-1601-9135 TABLET, FILM COATED in 1 BOTTLE (71335-1601-9)Feb 14, 2022

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