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Demeclocycline Hydrochloride

NDC 24658-710 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPuraCap Laboratories LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065447
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDEMECLOCYCLINE HYDROCHLORIDE (150 mg/1)
Marketing started20171007
Package count1

External sources

Source: openFDA. Public-domain (CC0).