NDC 63187-010 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-010

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077662
Marketed since
April 1, 2006
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
63187-010-3030 TABLET in 1 BOTTLE (63187-010-30)Dec 1, 2016
63187-010-6060 TABLET in 1 BOTTLE (63187-010-60)Apr 1, 2014
63187-010-9090 TABLET in 1 BOTTLE (63187-010-90)Apr 1, 2014

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