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DOXYCYCLINE HYCLATE

NDC 43547-325 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerSolco Healthcare US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207494
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDOXYCYCLINE HYCLATE (200 mg/1)
Marketing started20161128
Package count3

External sources

Source: openFDA. Public-domain (CC0).