NDC 71335-3060 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3060

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217995
Marketed since
April 4, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-3060-028 TABLET in 1 BOTTLE (71335-3060-0)Feb 5, 2026
71335-3060-130 TABLET in 1 BOTTLE (71335-3060-1)Feb 5, 2026
71335-3060-260 TABLET in 1 BOTTLE (71335-3060-2)Feb 5, 2026
71335-3060-3180 TABLET in 1 BOTTLE (71335-3060-3)Feb 5, 2026
71335-3060-490 TABLET in 1 BOTTLE (71335-3060-4)Feb 5, 2026
71335-3060-5100 TABLET in 1 BOTTLE (71335-3060-5)Feb 5, 2026
71335-3060-6120 TABLET in 1 BOTTLE (71335-3060-6)Feb 5, 2026
71335-3060-7500 TABLET in 1 BOTTLE (71335-3060-7)Feb 5, 2026
71335-3060-884 TABLET in 1 BOTTLE (71335-3060-8)Feb 5, 2026
71335-3060-9112 TABLET in 1 BOTTLE (71335-3060-9)Feb 5, 2026

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