FDA NDC Directory · JSON-LD · Markdown

Pseudoephedrine hydrochloride

NDC 51660-492 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic namepseudoephedrine hydrochloride
Labeler / ManufacturerOhm Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077442
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20060428
Package count1

External sources

Source: openFDA. Public-domain (CC0).