NDC 71205-932 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-932

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
71205-932-00100 TABLET in 1 BOTTLE (71205-932-00)Apr 22, 2021
71205-932-3030 TABLET in 1 BOTTLE (71205-932-30)Apr 22, 2021
71205-932-55500 TABLET in 1 BOTTLE (71205-932-55)Apr 22, 2021
71205-932-6060 TABLET in 1 BOTTLE (71205-932-60)Apr 22, 2021
71205-932-64240 TABLET in 1 BOTTLE (71205-932-64)Apr 22, 2021
71205-932-67270 TABLET in 1 BOTTLE (71205-932-67)Jun 28, 2021
71205-932-72120 TABLET in 1 BOTTLE (71205-932-72)Apr 22, 2021
71205-932-76360 TABLET in 1 BOTTLE (71205-932-76)Jun 28, 2021
71205-932-78180 TABLET in 1 BOTTLE (71205-932-78)Apr 22, 2021
71205-932-9090 TABLET in 1 BOTTLE (71205-932-90)Apr 22, 2021

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