NDC 72162-1531 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-1531

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
February 4, 2016
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
72162-1531-1100 TABLET in 1 BOTTLE (72162-1531-1)Aug 20, 2018
72162-1531-5500 TABLET in 1 BOTTLE (72162-1531-5)Aug 20, 2018

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