NDC 71335-0820 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0820

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078428
Marketed since
November 24, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0820-190 CAPSULE in 1 BOTTLE (71335-0820-1)Aug 1, 2018
71335-0820-228 CAPSULE in 1 BOTTLE (71335-0820-2)Oct 30, 2024
71335-0820-3120 CAPSULE in 1 BOTTLE (71335-0820-3)Oct 30, 2024
71335-0820-430 CAPSULE in 1 BOTTLE (71335-0820-4)Oct 30, 2024
71335-0820-560 CAPSULE in 1 BOTTLE (71335-0820-5)Oct 30, 2024

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