NDC 55289-959 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC55289-959

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077662
Marketed since
April 1, 2006
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
55289-959-3030 TABLET in 1 BOTTLE, PLASTIC (55289-959-30)Jan 27, 2020
55289-959-6060 TABLET in 1 BOTTLE, PLASTIC (55289-959-60)Oct 10, 2011
55289-959-9090 TABLET in 1 BOTTLE, PLASTIC (55289-959-90)Oct 10, 2011
55289-959-98120 TABLET in 1 BOTTLE, PLASTIC (55289-959-98)Oct 10, 2011

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