Package 62756-915-62

{"route": ["ORAL"], "spl_id": "a0bd1e9b-eb9f-46e7-8cee-10bde092d7cb", "openfda": {"unii": ["64O047KTOA", "6V9V2RYJ8N"], "rxcui": ["1014571"], "spl_set_id": ["796c4b81-145b-4050-a851-dec81ff97006"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (62756-915-62)  / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (62756-915-60)", "package_ndc": "62756-915-62", "marketing_start_date": "20120929"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (62756-915-73)  / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (62756-915-60)", "package_ndc": "62756-915-73", "marketing_start_date": "20120929"}], "brand_name": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "62756-915_a0bd1e9b-eb9f-46e7-8cee-10bde092d7cb", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "62756-915", "generic_name": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090922", "marketing_category": "ANDA", "marketing_start_date": "20120929", "listing_expiration_date": "20261231"}