NDC 63187-057 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-057

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 (4)

Package NDCDescriptionSince
63187-057-00100 TABLET in 1 BOTTLE (63187-057-00)Jun 2, 2014
63187-057-3030 TABLET in 1 BOTTLE (63187-057-30)Jun 1, 2014
63187-057-6060 TABLET in 1 BOTTLE (63187-057-60)Jun 2, 2014
63187-057-9090 TABLET in 1 BOTTLE (63187-057-90)Jun 2, 2014

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