NDC 71335-1200 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1200

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, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1200-028 TABLET in 1 BOTTLE (71335-1200-0)Jan 30, 2025
71335-1200-130 TABLET in 1 BOTTLE (71335-1200-1)May 6, 2019
71335-1200-260 TABLET in 1 BOTTLE (71335-1200-2)May 13, 2019
71335-1200-3180 TABLET in 1 BOTTLE (71335-1200-3)Jun 12, 2019
71335-1200-490 TABLET in 1 BOTTLE (71335-1200-4)Apr 22, 2019
71335-1200-5100 TABLET in 1 BOTTLE (71335-1200-5)Jan 30, 2025
71335-1200-6120 TABLET in 1 BOTTLE (71335-1200-6)May 2, 2019
71335-1200-7500 TABLET in 1 BOTTLE (71335-1200-7)Jan 30, 2025
71335-1200-884 TABLET in 1 BOTTLE (71335-1200-8)Jan 30, 2025
71335-1200-9112 TABLET in 1 BOTTLE (71335-1200-9)Jan 30, 2025

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