NDC 71335-2037 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2037

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206402
Marketed since
November 1, 2015
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (9)

Package NDCDescriptionSince
71335-2037-130 TABLET in 1 BOTTLE (71335-2037-1)Apr 13, 2022
71335-2037-260 TABLET in 1 BOTTLE (71335-2037-2)Mar 7, 2022
71335-2037-390 TABLET in 1 BOTTLE (71335-2037-3)Mar 7, 2022
71335-2037-4180 TABLET in 1 BOTTLE (71335-2037-4)Jan 30, 2025
71335-2037-5120 TABLET in 1 BOTTLE (71335-2037-5)Mar 14, 2022
71335-2037-6100 TABLET in 1 BOTTLE (71335-2037-6)Jan 30, 2025
71335-2037-784 TABLET in 1 BOTTLE (71335-2037-7)Jan 30, 2025
71335-2037-8112 TABLET in 1 BOTTLE (71335-2037-8)Jan 30, 2025
71335-2037-9135 TABLET in 1 BOTTLE (71335-2037-9)Jan 30, 2025

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