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Doxycycline

NDC 70710-1122 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209582
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDOXYCYCLINE (75 mg/1)
Marketing started20180111
Package count1

External sources

Source: openFDA. Public-domain (CC0).