NDC 71335-2048 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2048

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206402
Marketed since
November 1, 2015
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (6)

Package NDCDescriptionSince
71335-2048-190 TABLET in 1 BOTTLE (71335-2048-1)Mar 15, 2022
71335-2048-258 TABLET in 1 BOTTLE (71335-2048-2)Jan 30, 2025
71335-2048-3100 TABLET in 1 BOTTLE (71335-2048-3)Dec 27, 2022
71335-2048-4120 TABLET in 1 BOTTLE (71335-2048-4)Mar 22, 2022
71335-2048-560 TABLET in 1 BOTTLE (71335-2048-5)Feb 21, 2022
71335-2048-630 TABLET in 1 BOTTLE (71335-2048-6)Jun 21, 2023

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