NDC 71205-532 – Gabapentin

Gabapentin 300 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-532

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 (6)

Package NDCDescriptionSince
71205-532-1414 CAPSULE in 1 BOTTLE (71205-532-14)Jan 5, 2022
71205-532-1515 CAPSULE in 1 BOTTLE (71205-532-15)Feb 4, 2021
71205-532-3030 CAPSULE in 1 BOTTLE (71205-532-30)Feb 4, 2021
71205-532-6060 CAPSULE in 1 BOTTLE (71205-532-60)Feb 4, 2021
71205-532-72120 CAPSULE in 1 BOTTLE (71205-532-72)May 25, 2021
71205-532-9090 CAPSULE in 1 BOTTLE (71205-532-90)Feb 4, 2021

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