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Doxycycline Hyclate

NDC 53489-647 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065134
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDOXYCYCLINE HYCLATE (20 mg/1)
Marketing started20050513
Package count7

External sources

Source: openFDA. Public-domain (CC0).