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Methotrexate

NDC 0143-9517 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA089342
Dosage form / routeSOLUTION · INTRA-ARTERIAL INTRAMUSCULAR INTRATHECAL INTRAVENOUS
Active ingredientsMETHOTREXATE (25 mg/mL)
Marketing started20180105
Package count1

External sources

Source: openFDA. Public-domain (CC0).