NDC 71205-930 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-930

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204989
Marketed since
April 1, 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
71205-930-00100 CAPSULE in 1 BOTTLE (71205-930-00)Apr 22, 2021
71205-930-3030 CAPSULE in 1 BOTTLE (71205-930-30)Apr 22, 2021
71205-930-55500 CAPSULE in 1 BOTTLE (71205-930-55)Apr 22, 2021
71205-930-6060 CAPSULE in 1 BOTTLE (71205-930-60)Apr 22, 2021
71205-930-64240 CAPSULE in 1 BOTTLE (71205-930-64)Apr 22, 2021
71205-930-67270 CAPSULE in 1 BOTTLE (71205-930-67)Jun 28, 2021
71205-930-72120 CAPSULE in 1 BOTTLE (71205-930-72)Apr 22, 2021
71205-930-76360 CAPSULE in 1 BOTTLE (71205-930-76)Jun 28, 2021
71205-930-78180 CAPSULE in 1 BOTTLE (71205-930-78)Apr 22, 2021
71205-930-9090 CAPSULE in 1 BOTTLE (71205-930-90)Apr 22, 2021

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