NDC 71205-064 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-064

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA075350
Marketed since
April 3, 2014
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
71205-064-3030 CAPSULE in 1 BOTTLE (71205-064-30)Jul 2, 2018
71205-064-6060 CAPSULE in 1 BOTTLE (71205-064-60)Jul 2, 2018
71205-064-72120 CAPSULE in 1 BOTTLE (71205-064-72)Jul 2, 2018
71205-064-9090 CAPSULE in 1 BOTTLE (71205-064-90)Jul 2, 2018

Other Gabapentin products