NDC 71610-044 – Gabapentin

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

Human Prescription Drug

Product NDC71610-044

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203244
Marketed since
January 11, 2014
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (8)

Package NDCDescriptionSince
71610-044-3030 TABLET, FILM COATED in 1 BOTTLE (71610-044-30)Jun 10, 2020
71610-044-4545 TABLET, FILM COATED in 1 BOTTLE (71610-044-45)Jun 10, 2020
71610-044-5360 TABLET, FILM COATED in 1 BOTTLE (71610-044-53)Jun 10, 2020
71610-044-6090 TABLET, FILM COATED in 1 BOTTLE (71610-044-60)Mar 23, 2018
71610-044-70120 TABLET, FILM COATED in 1 BOTTLE (71610-044-70)Jul 30, 2020
71610-044-73135 TABLET, FILM COATED in 1 BOTTLE (71610-044-73)Jul 30, 2020
71610-044-80180 TABLET, FILM COATED in 1 BOTTLE (71610-044-80)Mar 23, 2018
71610-044-92270 TABLET, FILM COATED in 1 BOTTLE (71610-044-92)Mar 23, 2018

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