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Methotrexate

NDC 0703-3675 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerTeva Parenteral Medicines, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040843
Dosage form / routeINJECTION, SOLUTION · INTRA-ARTERIAL INTRAMUSCULAR INTRATHECAL INTRAVENOUS
Active ingredientsMETHOTREXATE SODIUM (25 mg/mL)
Marketing started20120801
Package count1

External sources

Source: openFDA. Public-domain (CC0).