NDC 71335-1199 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1199

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA090858
Marketed since
January 29, 2011
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1199-0180 CAPSULE in 1 BOTTLE (71335-1199-0)Aug 19, 2026
71335-1199-120 CAPSULE in 1 BOTTLE (71335-1199-1)Aug 19, 2026
71335-1199-290 CAPSULE in 1 BOTTLE (71335-1199-2)May 7, 2019
71335-1199-360 CAPSULE in 1 BOTTLE (71335-1199-3)May 2, 2019
71335-1199-430 CAPSULE in 1 BOTTLE (71335-1199-4)May 29, 2019
71335-1199-5120 CAPSULE in 1 BOTTLE (71335-1199-5)Feb 11, 2022
71335-1199-621 CAPSULE in 1 BOTTLE (71335-1199-6)Aug 19, 2026
71335-1199-784 CAPSULE in 1 BOTTLE (71335-1199-7)Aug 19, 2026
71335-1199-8112 CAPSULE in 1 BOTTLE (71335-1199-8)Aug 19, 2026
71335-1199-928 CAPSULE in 1 BOTTLE (71335-1199-9)Aug 19, 2026

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