Package 55910-699-66

Brand: rexall all day allergy relief

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55910-699-66
Digits Only 5591069966
Product NDC 55910-699
Description

1 BLISTER PACK in 1 CARTON (55910-699-66) / 14 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-09-06
Brand rexall all day allergy relief
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eba98b0b-bc85-4d05-8875-86b85bd462b4", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["4d79fb74-1895-4efe-8016-c0dd5ed10f7a"], "manufacturer_name": ["Dolgencorp, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (55910-699-66)  / 14 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55910-699-66", "marketing_start_date": "20120906"}], "brand_name": "rexall all day allergy relief", "product_id": "55910-699_eba98b0b-bc85-4d05-8875-86b85bd462b4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55910-699", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Dolgencorp, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "rexall all day allergy relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20120906", "listing_expiration_date": "20261231"}