NDC 60760-837 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60760-837

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
October 1, 2021
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
60760-837-6060 TABLET in 1 BOTTLE, PLASTIC (60760-837-60)Mar 18, 2026

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