NDC 71335-1287 – Gabapentin

Gabapentin 600 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-1287

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207057
Marketed since
May 1, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1287-028 TABLET, COATED in 1 BOTTLE (71335-1287-0)Dec 28, 2021
71335-1287-130 TABLET, COATED in 1 BOTTLE (71335-1287-1)Dec 28, 2021
71335-1287-260 TABLET, COATED in 1 BOTTLE (71335-1287-2)Aug 21, 2019
71335-1287-3180 TABLET, COATED in 1 BOTTLE (71335-1287-3)Dec 28, 2021
71335-1287-490 TABLET, COATED in 1 BOTTLE (71335-1287-4)Aug 28, 2019
71335-1287-5100 TABLET, COATED in 1 BOTTLE (71335-1287-5)Dec 28, 2021
71335-1287-6120 TABLET, COATED in 1 BOTTLE (71335-1287-6)Aug 27, 2019
71335-1287-7500 TABLET, COATED in 1 BOTTLE (71335-1287-7)Dec 28, 2021
71335-1287-884 TABLET, COATED in 1 BOTTLE (71335-1287-8)Dec 28, 2021
71335-1287-9112 TABLET, COATED in 1 BOTTLE (71335-1287-9)Dec 28, 2021

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