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Liothyronine Sodium

NDC 68071-3571 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200295
Dosage form / routeTABLET · ORAL
Active ingredientsLIOTHYRONINE SODIUM (5 ug/1)
Marketing started20121203
Package count1

External sources

Source: openFDA. Public-domain (CC0).