NDC 71335-2819 – Gabapentin

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

Human Prescription Drug

Product NDC71335-2819

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 (6)

Package NDCDescriptionSince
71335-2819-190 TABLET, FILM COATED in 1 BOTTLE (71335-2819-1)Oct 22, 2025
71335-2819-218 TABLET, FILM COATED in 1 BOTTLE (71335-2819-2)Oct 22, 2025
71335-2819-358 TABLET, FILM COATED in 1 BOTTLE (71335-2819-3)Oct 22, 2025
71335-2819-460 TABLET, FILM COATED in 1 BOTTLE (71335-2819-4)Oct 22, 2025
71335-2819-530 TABLET, FILM COATED in 1 BOTTLE (71335-2819-5)Oct 22, 2025
71335-2819-6120 TABLET, FILM COATED in 1 BOTTLE (71335-2819-6)Oct 22, 2025

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