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Loratadine and Pseudoephedrine Sulfate

NDC 0904-5833 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA076557
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLORATADINE (10 mg/1)
PSEUDOEPHEDRINE SULFATE (240 mg/1)
Marketing started20041117
Package count2

External sources

Source: openFDA. Public-domain (CC0).