potassium chloride

Generic: potassium chloride

Labeler: mckesson corporation dba sky packaginng
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler mckesson corporation dba sky packaginng
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Mckesson Corporation DBA SKY Packaginng

Identifiers & Regulatory

Product NDC 63739-972
Product ID 63739-972_2b4b7151-598a-5b5d-e063-6394a90ac32a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074726
Marketing Start 1998-11-20
Marketing End 2026-08-31

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739972
Hyphenated Format 63739-972

Supplemental Identifiers

RxCUI
1801294 1801298
UNII
660YQ98I10

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA074726 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-972-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

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

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

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"}