Package 63739-972-10

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 63739-972-10
Digits Only 6373997210
Product NDC 63739-972
Product ID 63739-972_2b4b7151-598a-5b5d-e063-6394a90ac32a
Description

10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-972-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-08-31
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": "2b4b7151-598a-5b5d-e063-6394a90ac32a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["5cccc39f-6a6d-415e-a55f-f4ee57f72a0a"], "manufacturer_name": ["Mckesson Corporation DBA SKY Packaginng"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-972-10)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63739-972-10", "marketing_end_date": "20260831", "marketing_start_date": "19981120"}], "brand_name": "Potassium Chloride", "product_id": "63739-972_2b4b7151-598a-5b5d-e063-6394a90ac32a", "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": "63739-972", "generic_name": "potassium chloride", "labeler_name": "Mckesson Corporation DBA SKY Packaginng", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "19981120"}