FDA NDC Directory · JSON-LD · Markdown

signature care allergy relief d

NDC 21130-644 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namecetirizine hydrochloride, pseudoephedrine hydrochloride
Labeler / ManufacturerSafeway
Marketing categoryAbbreviated NDA (generic) · App ANDA210719
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20210216
Package count1

External sources

Source: openFDA. Public-domain (CC0).