Package 63304-076-01

{"route": ["ORAL"], "spl_id": "0e924cf6-53b8-28c4-e063-6294a90a4ac4", "openfda": {"upc": ["0363304076011"], "unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["8ed8ea55-8b15-f718-e053-2a95a90a587a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-01)", "package_ndc": "63304-076-01", "marketing_start_date": "20191120"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-05)", "package_ndc": "63304-076-05", "marketing_start_date": "20191120"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-10)", "package_ndc": "63304-076-10", "marketing_start_date": "20191120"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "63304-076_0e924cf6-53b8-28c4-e063-6294a90a4ac4", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "63304-076", "generic_name": "Potassium Chloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076368", "marketing_category": "ANDA", "marketing_start_date": "20191120", "listing_expiration_date": "20261231"}