Package 70518-3525-0

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 70518-3525-0
Digits Only 7051835250
Product NDC 70518-3525
Product ID 70518-3525_3ab05224-bc22-e501-e063-6294a90a7d7b
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3525-0)

Marketing

Marketing Status
Marketed Since 2022-09-17
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ab05224-bc22-e501-e063-6294a90a7d7b", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["4270cce8-4cbb-4d67-a4cb-f073ef554d12"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3525-0)", "package_ndc": "70518-3525-0", "marketing_start_date": "20220917"}], "brand_name": "Potassium Chloride", "product_id": "70518-3525_3ab05224-bc22-e501-e063-6294a90a7d7b", "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": "70518-3525", "generic_name": "Potassium Chloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA212861", "marketing_category": "ANDA", "marketing_start_date": "20220917", "listing_expiration_date": "20261231"}