NDC 71610-069 – Gabapentin

Gabapentin 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71610-069

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077525
Marketed since
August 24, 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
71610-069-4545 TABLET, FILM COATED in 1 BOTTLE (71610-069-45)Feb 26, 2021
71610-069-6090 TABLET, FILM COATED in 1 BOTTLE (71610-069-60)May 15, 2018
71610-069-80180 TABLET, FILM COATED in 1 BOTTLE (71610-069-80)May 15, 2018
71610-069-92270 TABLET, FILM COATED in 1 BOTTLE (71610-069-92)May 15, 2018

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