NDC 71205-808 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-808

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

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
71205-808-3030 CAPSULE in 1 BOTTLE (71205-808-30)May 25, 2023
71205-808-6060 CAPSULE in 1 BOTTLE (71205-808-60)May 25, 2023
71205-808-9090 CAPSULE in 1 BOTTLE (71205-808-90)May 25, 2023

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