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Levothyroxine Sodium

NDC 70511-113 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameLEVOTHYROXINE SODIUM ANHYDROUS
Labeler / ManufacturerMAIA Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208749
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsLEVOTHYROXINE SODIUM ANHYDROUS (500 ug/5mL)
Marketing started20181227
Package count1

External sources

Source: openFDA. Public-domain (CC0).