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Doxycycline

NDC 0527-1537 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065285
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDOXYCYCLINE (150 mg/1)
Marketing started20080825
Package count2

External sources

Source: openFDA. Public-domain (CC0).