NDC 71335-2038 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2038

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
71335-2038-190 TABLET in 1 BOTTLE (71335-2038-1)Mar 7, 2022
71335-2038-218 TABLET in 1 BOTTLE (71335-2038-2)Jan 30, 2025
71335-2038-358 TABLET in 1 BOTTLE (71335-2038-3)Jan 30, 2025
71335-2038-460 TABLET in 1 BOTTLE (71335-2038-4)Mar 27, 2023
71335-2038-530 TABLET in 1 BOTTLE (71335-2038-5)Jan 26, 2022
71335-2038-6120 TABLET in 1 BOTTLE (71335-2038-6)Feb 1, 2022

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