Package 55910-699-66
Brand: rexall all day allergy relief
Generic: cetirizine hydrochloridePackage 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
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"}