NDC 71205-931 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-931

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 (10)

Package NDCDescriptionSince
71205-931-00100 TABLET in 1 BOTTLE (71205-931-00)Apr 22, 2021
71205-931-3030 TABLET in 1 BOTTLE (71205-931-30)Apr 22, 2021
71205-931-55500 TABLET in 1 BOTTLE (71205-931-55)Apr 22, 2021
71205-931-6060 TABLET in 1 BOTTLE (71205-931-60)Apr 22, 2021
71205-931-64240 TABLET in 1 BOTTLE (71205-931-64)Apr 22, 2021
71205-931-67270 TABLET in 1 BOTTLE (71205-931-67)Jun 28, 2021
71205-931-72120 TABLET in 1 BOTTLE (71205-931-72)Apr 22, 2021
71205-931-76360 TABLET in 1 BOTTLE (71205-931-76)Jun 28, 2021
71205-931-78180 TABLET in 1 BOTTLE (71205-931-78)Apr 22, 2021
71205-931-9090 TABLET in 1 BOTTLE (71205-931-90)Apr 22, 2021

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