NDC 71335-0351 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0351

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA075350
Marketed since
April 3, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0351-0180 CAPSULE in 1 BOTTLE (71335-0351-0)Oct 8, 2024
71335-0351-120 CAPSULE in 1 BOTTLE (71335-0351-1)Oct 8, 2024
71335-0351-290 CAPSULE in 1 BOTTLE (71335-0351-2)Mar 21, 2018
71335-0351-360 CAPSULE in 1 BOTTLE (71335-0351-3)May 29, 2018
71335-0351-430 CAPSULE in 1 BOTTLE (71335-0351-4)May 15, 2018
71335-0351-5120 CAPSULE in 1 BOTTLE (71335-0351-5)Mar 7, 2018
71335-0351-621 CAPSULE in 1 BOTTLE (71335-0351-6)Oct 8, 2024
71335-0351-784 CAPSULE in 1 BOTTLE (71335-0351-7)Oct 8, 2024
71335-0351-8112 CAPSULE in 1 BOTTLE (71335-0351-8)Oct 8, 2024
71335-0351-928 CAPSULE in 1 BOTTLE (71335-0351-9)Oct 8, 2024

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