Package 51660-939-30

{"route": ["ORAL"], "spl_id": "2a87ee90-da59-4e35-9cda-27759ba080d4", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["161c4122-2c89-46e6-a6ae-db088087330d"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51660-939-01)", "package_ndc": "51660-939-01", "marketing_start_date": "20071227"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (51660-939-13)", "package_ndc": "51660-939-13", "marketing_start_date": "20071227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51660-939-30)", "package_ndc": "51660-939-30", "marketing_start_date": "20071227"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (51660-939-53)", "package_ndc": "51660-939-53", "marketing_start_date": "20071227"}, {"sample": false, "description": "14 TABLET in 1 BLISTER PACK (51660-939-54)", "package_ndc": "51660-939-54", "marketing_start_date": "20071227"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (51660-939-90)", "package_ndc": "51660-939-90", "marketing_start_date": "20071227"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "51660-939_2a87ee90-da59-4e35-9cda-27759ba080d4", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51660-939", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077498", "marketing_category": "ANDA", "marketing_start_date": "20071227", "listing_expiration_date": "20261231"}