NDC 71205-533 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-533

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
February 4, 2016
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
71205-533-3030 TABLET in 1 BOTTLE (71205-533-30)Feb 9, 2021
71205-533-6060 TABLET in 1 BOTTLE (71205-533-60)Feb 9, 2021
71205-533-9090 TABLET in 1 BOTTLE (71205-533-90)Feb 9, 2021

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