Package 62207-726-49

{"route": ["ORAL"], "spl_id": "44e29e92-b045-b2f8-e063-6394a90a7f6a", "openfda": {"upc": ["0362207727495"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["60285a8d-bcb0-40ba-b359-df5c89480cd6"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62207-726-43)", "package_ndc": "62207-726-43", "marketing_start_date": "20210130"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62207-726-47)", "package_ndc": "62207-726-47", "marketing_start_date": "20210130"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62207-726-49)", "package_ndc": "62207-726-49", "marketing_start_date": "20210130"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62207-726-57)", "package_ndc": "62207-726-57", "marketing_start_date": "20210130"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "62207-726_44e29e92-b045-b2f8-e063-6394a90a7f6a", "dosage_form": "TABLET", "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": "62207-726", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Granules India Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}