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Droxidopa

NDC 70771-1609 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211818
Dosage form / routeCAPSULE · ORAL
Active ingredientsDROXIDOPA (100 mg/1)
Marketing started20210219
Package count1

External sources

Source: openFDA. Public-domain (CC0).