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Pilocarpine Hydrochloride

NDC 0527-1407 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077220
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPILOCARPINE HYDROCHLORIDE (7.5 mg/1)
Marketing started20051014
Package count1

External sources

Source: openFDA. Public-domain (CC0).