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meloxicam

NDC 35356-808 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerQuality Care Products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077927
Dosage form / routeTABLET · ORAL
Active ingredientsMELOXICAM (7.5 mg/1)
Marketing started20070307
Marketing ended20261231
Package count3

External sources

Source: openFDA. Public-domain (CC0).