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Meloxicam

NDC 71205-923 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077918
Dosage form / routeTABLET · ORAL
Active ingredientsMELOXICAM (7.5 mg/1)
Marketing started20100630
Package count11

External sources

Source: openFDA. Public-domain (CC0).