Package 64380-861-08

{"route": ["ORAL"], "spl_id": "a74390de-64e9-482d-8630-d1a2452324fe", "openfda": {"upc": ["0364380861065", "0364380860068"], "unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["0224e5b3-3c49-4e6e-aa78-1abcc6969246"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-06)", "package_ndc": "64380-861-06", "marketing_start_date": "20181127"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-07)", "package_ndc": "64380-861-07", "marketing_start_date": "20181127"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-08)", "package_ndc": "64380-861-08", "marketing_start_date": "20181127"}], "brand_name": "Potassium Chloride", "product_id": "64380-861_a74390de-64e9-482d-8630-d1a2452324fe", "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": "64380-861", "generic_name": "Potassium Chloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210733", "marketing_category": "ANDA", "marketing_start_date": "20181127", "listing_expiration_date": "20261231"}