Package 43598-160-53

{"route": ["ORAL"], "spl_id": "21ff31d2-239a-4997-b999-3b7cc55994b9", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["dda82a38-0c08-4947-99b7-915c2949bf16"], "manufacturer_name": ["Dr. Reddys Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-01)  / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31)", "package_ndc": "43598-160-01", "marketing_start_date": "20220725"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-53)  / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31)", "package_ndc": "43598-160-53", "marketing_start_date": "20220725"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "43598-160_21ff31d2-239a-4997-b999-3b7cc55994b9", "dosage_form": "SOLUTION", "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": "43598-160", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Dr. Reddys Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/30mL"}], "application_number": "ANDA213062", "marketing_category": "ANDA", "marketing_start_date": "20220725", "listing_expiration_date": "20261231"}