Package 51655-194-26

{"route": ["ORAL"], "spl_id": "48c43399-eff4-c940-e063-6394a90aacd9", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["f2b4d221-30ae-5a43-e053-2995a90a238a"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-26)", "package_ndc": "51655-194-26", "marketing_start_date": "20221115"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-52)", "package_ndc": "51655-194-52", "marketing_start_date": "20230302"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-60)", "package_ndc": "51655-194-60", "marketing_start_date": "20221018"}], "brand_name": "Cetirizine", "product_id": "51655-194_48c43399-eff4-c940-e063-6394a90aacd9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51655-194", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20221018", "listing_expiration_date": "20271231"}