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Clarithromycin

NDC 0527-1932 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203584
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCLARITHROMYCIN (500 mg/1)
Marketing started20191123
Package count1

External sources

Source: openFDA. Public-domain (CC0).