NDC 71335-0254 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0254

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077662
Marketed since
April 1, 2006
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (9)

Package NDCDescriptionSince
71335-0254-130 TABLET in 1 BOTTLE (71335-0254-1)Jul 19, 2018
71335-0254-260 TABLET in 1 BOTTLE (71335-0254-2)May 4, 2018
71335-0254-390 TABLET in 1 BOTTLE (71335-0254-3)Mar 15, 2018
71335-0254-4180 TABLET in 1 BOTTLE (71335-0254-4)May 11, 2018
71335-0254-5120 TABLET in 1 BOTTLE (71335-0254-5)Apr 17, 2018
71335-0254-6100 TABLET in 1 BOTTLE (71335-0254-6)Oct 8, 2024
71335-0254-784 TABLET in 1 BOTTLE (71335-0254-7)Apr 3, 2018
71335-0254-8112 TABLET in 1 BOTTLE (71335-0254-8)Oct 8, 2024
71335-0254-9135 TABLET in 1 BOTTLE (71335-0254-9)Oct 8, 2024

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