NDC 71335-3143 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3143

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 (6)

Package NDCDescriptionSince
71335-3143-190 TABLET in 1 BOTTLE (71335-3143-1)Jun 18, 2026
71335-3143-258 TABLET in 1 BOTTLE (71335-3143-2)Jun 18, 2026
71335-3143-3100 TABLET in 1 BOTTLE (71335-3143-3)Jun 18, 2026
71335-3143-4120 TABLET in 1 BOTTLE (71335-3143-4)Jun 18, 2026
71335-3143-560 TABLET in 1 BOTTLE (71335-3143-5)Jun 18, 2026
71335-3143-630 TABLET in 1 BOTTLE (71335-3143-6)Jun 18, 2026

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