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Doxycycline

NDC 63304-173 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSun Pharmaceutical Industries Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065356
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDOXYCYCLINE (150 mg/1)
Marketing started20180806
Package count4

External sources

Source: openFDA. Public-domain (CC0).