NDC 71205-457 – Gabapentin

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

Human Prescription Drug

Product NDC71205-457

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
71205-457-3030 TABLET, FILM COATED in 1 BOTTLE (71205-457-30)Jun 23, 2020
71205-457-6060 TABLET, FILM COATED in 1 BOTTLE (71205-457-60)Jun 23, 2020
71205-457-9090 TABLET, FILM COATED in 1 BOTTLE (71205-457-90)Jun 23, 2020

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