Package 30142-058-76
Brand: cetirizine hydrochloride
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
30142-058-76
Digits Only
3014205876
Product NDC
30142-058
Description
4 BLISTER PACK in 1 CARTON (30142-058-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing
Marketing Status
Brand
cetirizine hydrochloride
Generic
cetirizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "013f034c-15f9-4da2-b74c-ac999b276053", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1011482"], "spl_set_id": ["b8b2af96-af48-5f63-e053-2995a90a7d7c"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (30142-058-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "30142-058-76", "marketing_start_date": "20210308"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "30142-058_013f034c-15f9-4da2-b74c-ac999b276053", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "30142-058", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213557", "marketing_category": "ANDA", "marketing_start_date": "20210308", "listing_expiration_date": "20261231"}