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Gabapentin

NDC 80425-0033 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090858
Dosage form / routeCAPSULE · ORAL
Active ingredientsGABAPENTIN (300 mg/1)
Marketing started20110129
Package count6

External sources

Source: openFDA. Public-domain (CC0).