NDC 71335-0214 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0214

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 (10)

Package NDCDescriptionSince
71335-0214-0180 CAPSULE in 1 BOTTLE (71335-0214-0)Oct 30, 2024
71335-0214-120 CAPSULE in 1 BOTTLE (71335-0214-1)Oct 30, 2024
71335-0214-290 CAPSULE in 1 BOTTLE (71335-0214-2)Apr 11, 2018
71335-0214-360 CAPSULE in 1 BOTTLE (71335-0214-3)Jun 4, 2018
71335-0214-430 CAPSULE in 1 BOTTLE (71335-0214-4)Jul 3, 2018
71335-0214-5120 CAPSULE in 1 BOTTLE (71335-0214-5)Aug 27, 2018
71335-0214-621 CAPSULE in 1 BOTTLE (71335-0214-6)Oct 30, 2024
71335-0214-784 CAPSULE in 1 BOTTLE (71335-0214-7)Oct 30, 2024
71335-0214-8112 CAPSULE in 1 BOTTLE (71335-0214-8)Oct 30, 2024
71335-0214-928 CAPSULE in 1 BOTTLE (71335-0214-9)Oct 30, 2024

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