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Meloxicam

NDC 80425-0559 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077882
Dosage form / routeTABLET · ORAL
Active ingredientsMELOXICAM (7.5 mg/1)
Marketing started20251124
Package count4

External sources

Source: openFDA. Public-domain (CC0).