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Acetaminophen and Codeine Phosphate

NDC 68071-5010 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202800
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (300 mg/1)
CODEINE PHOSPHATE (30 mg/1)
Marketing started20130415
Package count2

External sources

Source: openFDA. Public-domain (CC0).