NDC 71205-774 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-774

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
April 11, 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
71205-774-3030 TABLET in 1 BOTTLE (71205-774-30)Mar 14, 2023
71205-774-6060 TABLET in 1 BOTTLE (71205-774-60)Mar 14, 2023
71205-774-9090 TABLET in 1 BOTTLE (71205-774-90)Mar 14, 2023

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