NDC 71335-3057 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3057

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
October 1, 2021
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (9)

Package NDCDescriptionSince
71335-3057-130 TABLET in 1 BOTTLE (71335-3057-1)Feb 6, 2026
71335-3057-260 TABLET in 1 BOTTLE (71335-3057-2)Feb 6, 2026
71335-3057-390 TABLET in 1 BOTTLE (71335-3057-3)Feb 6, 2026
71335-3057-4180 TABLET in 1 BOTTLE (71335-3057-4)Feb 6, 2026
71335-3057-5120 TABLET in 1 BOTTLE (71335-3057-5)Feb 6, 2026
71335-3057-6100 TABLET in 1 BOTTLE (71335-3057-6)Feb 6, 2026
71335-3057-784 TABLET in 1 BOTTLE (71335-3057-7)Feb 6, 2026
71335-3057-8112 TABLET in 1 BOTTLE (71335-3057-8)Feb 6, 2026
71335-3057-9135 TABLET in 1 BOTTLE (71335-3057-9)Feb 6, 2026

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