Package 70010-136-01

{"route": ["ORAL"], "spl_id": "495d2e0b-e6b6-958e-e063-6394a90ac328", "openfda": {"upc": ["0370010135017"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["b3d4d5b5-2898-ae3d-e053-2a95a90a6d04"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-136-01)", "package_ndc": "70010-136-01", "marketing_start_date": "20210130"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-136-05)", "package_ndc": "70010-136-05", "marketing_start_date": "20210130"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-136-10)", "package_ndc": "70010-136-10", "marketing_start_date": "20210130"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "70010-136_495d2e0b-e6b6-958e-e063-6394a90ac328", "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": "70010-136", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Granules Pharmaceuticals Inc.", "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": "20271231"}