FDA NDC Directory · JSON-LD · Markdown

Codeine Sulfate

NDC 0527-1698 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203046
Dosage form / routeTABLET · ORAL
Active ingredientsCODEINE SULFATE (30 mg/1)
Marketing started20140613
Package count2

External sources

Source: openFDA. Public-domain (CC0).