NDC 71335-2700 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2700

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078787
Marketed since
January 31, 2008
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2700-0180 CAPSULE in 1 BOTTLE (71335-2700-0)Sep 25, 2025
71335-2700-120 CAPSULE in 1 BOTTLE (71335-2700-1)Sep 25, 2025
71335-2700-290 CAPSULE in 1 BOTTLE (71335-2700-2)Sep 25, 2025
71335-2700-360 CAPSULE in 1 BOTTLE (71335-2700-3)Sep 25, 2025
71335-2700-430 CAPSULE in 1 BOTTLE (71335-2700-4)Sep 25, 2025
71335-2700-5120 CAPSULE in 1 BOTTLE (71335-2700-5)Sep 25, 2025
71335-2700-621 CAPSULE in 1 BOTTLE (71335-2700-6)Sep 25, 2025
71335-2700-784 CAPSULE in 1 BOTTLE (71335-2700-7)Sep 25, 2025
71335-2700-8112 CAPSULE in 1 BOTTLE (71335-2700-8)Sep 25, 2025
71335-2700-928 CAPSULE in 1 BOTTLE (71335-2700-9)Sep 25, 2025

Other Gabapentin products