FDA NDC Directory · JSON-LD · Markdown

Loratadine and Pseudoephedrine

NDC 51660-491 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameloratadine and pseudoephedrine
Labeler / ManufacturerOhm Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076557
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsLORATADINE (10 mg/1)
PSEUDOEPHEDRINE SULFATE (240 mg/1)
Marketing started20041117
Package count1

External sources

Source: openFDA. Public-domain (CC0).