NDC 71335-2701 – Gabapentin

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

Human Prescription Drug

Product NDC71335-2701

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200651
Marketed since
October 6, 2011
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2701-028 TABLET, FILM COATED in 1 BOTTLE (71335-2701-0)Sep 26, 2025
71335-2701-130 TABLET, FILM COATED in 1 BOTTLE (71335-2701-1)Sep 26, 2025
71335-2701-260 TABLET, FILM COATED in 1 BOTTLE (71335-2701-2)Sep 26, 2025
71335-2701-3180 TABLET, FILM COATED in 1 BOTTLE (71335-2701-3)Sep 26, 2025
71335-2701-490 TABLET, FILM COATED in 1 BOTTLE (71335-2701-4)Sep 26, 2025
71335-2701-5100 TABLET, FILM COATED in 1 BOTTLE (71335-2701-5)Sep 26, 2025
71335-2701-6120 TABLET, FILM COATED in 1 BOTTLE (71335-2701-6)Sep 26, 2025
71335-2701-7500 TABLET, FILM COATED in 1 BOTTLE (71335-2701-7)Sep 26, 2025
71335-2701-884 TABLET, FILM COATED in 1 BOTTLE (71335-2701-8)Sep 26, 2025
71335-2701-9112 TABLET, FILM COATED in 1 BOTTLE (71335-2701-9)Sep 26, 2025

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