NDC 71335-1269 – Gabapentin

Gabapentin 300 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1269

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 (8)

Package NDCDescriptionSince
71335-1269-190 CAPSULE in 1 BOTTLE (71335-1269-1)Jul 11, 2019
71335-1269-228 CAPSULE in 1 BOTTLE (71335-1269-2)Aug 19, 2026
71335-1269-358 CAPSULE in 1 BOTTLE (71335-1269-3)Aug 19, 2026
71335-1269-430 CAPSULE in 1 BOTTLE (71335-1269-4)Jul 15, 2019
71335-1269-560 CAPSULE in 1 BOTTLE (71335-1269-5)Jul 9, 2019
71335-1269-6120 CAPSULE in 1 BOTTLE (71335-1269-6)Jul 31, 2019
71335-1269-7180 CAPSULE in 1 BOTTLE (71335-1269-7)Mar 29, 2023
71335-1269-840 CAPSULE in 1 BOTTLE (71335-1269-8)Mar 29, 2023

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