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Doxycycline

NDC 31722-371 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218888
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsDOXYCYCLINE HYCLATE (100 mg/10mL)
Marketing started20250805
Package count1

External sources

Source: openFDA. Public-domain (CC0).