NDC 76282-707 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76282-707

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Exelan Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
October 1, 2021
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
76282-707-05500 TABLET in 1 BOTTLE (76282-707-05)Oct 1, 2021
76282-707-9090 TABLET in 1 BOTTLE (76282-707-90)Oct 1, 2021

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