NDC 76282-323 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC76282-323

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Exelan Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA090705
Marketed since
April 26, 2010
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
76282-323-01100 CAPSULE in 1 BOTTLE (76282-323-01)Apr 26, 2010
76282-323-05500 CAPSULE in 1 BOTTLE (76282-323-05)Apr 26, 2010
76282-323-27270 CAPSULE in 1 BOTTLE (76282-323-27)Mar 20, 2013
76282-323-9090 CAPSULE in 1 BOTTLE (76282-323-90)Mar 20, 2013

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