Package 60687-632-01

{"route": ["ORAL"], "spl_id": "204bc844-c945-938e-e063-6294a90ad011", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["8c12c5f8-5950-44e3-9473-a0b95187b43c"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-632-01)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-632-11)", "package_ndc": "60687-632-01", "marketing_start_date": "20230302"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "60687-632_204bc844-c945-938e-e063-6294a90ad011", "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": "60687-632", "generic_name": "Potassium Chloride", "labeler_name": "American Health Packaging", "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": "20230302", "listing_expiration_date": "20261231"}