Package 68210-0119-0

{"route": ["ORAL"], "spl_id": "2a804c42-e22a-703e-e063-6394a90a3b1b", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["e49c3c91-aab8-478e-97fa-04ed06180021"], "manufacturer_name": ["Spirit Pharmaceutical LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0119-0)", "package_ndc": "68210-0119-0", "marketing_start_date": "20191025"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (68210-0119-1)", "package_ndc": "68210-0119-1", "marketing_start_date": "20200310"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3)  / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68210-0119-3", "marketing_start_date": "20200310"}], "brand_name": "CABINET Allergy Relief", "product_id": "68210-0119_2a804c42-e22a-703e-e063-6394a90a3b1b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68210-0119", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Spirit Pharmaceutical LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CABINET Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20191025", "listing_expiration_date": "20261231"}