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Gabapentin

NDC 80425-0201 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207057
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20221028
Package count4

External sources

Source: openFDA. Public-domain (CC0).