Package 0904-7462-43

{"route": ["ORAL"], "spl_id": "0e0defca-901d-4b4b-ac96-ac72fcfe4303", "openfda": {"upc": ["0309047461882", "0309047462629"], "unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["33ad1eb2-1f05-461c-b01d-82dee4231556"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (0904-7462-43)  / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-43", "marketing_end_date": "20270531", "marketing_start_date": "20240708"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CASE (0904-7462-60)  / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-60", "marketing_start_date": "20240708"}, {"sample": false, "description": "30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-62", "marketing_start_date": "20240708"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (0904-7462-73)  / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)", "package_ndc": "0904-7462-73", "marketing_start_date": "20240708"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "0904-7462_0e0defca-901d-4b4b-ac96-ac72fcfe4303", "dosage_form": "SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0904-7462", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/30mL"}], "application_number": "ANDA210766", "marketing_category": "ANDA", "marketing_start_date": "20240708", "listing_expiration_date": "20271231"}