potassium chloride
Generic: potassium chloride
Labeler: mckesson corporation dba sky packagingDrug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
mckesson corporation dba sky packaging
Dosage Form
SOLUTION
Routes
Active Ingredients
potassium chloride 20 meq/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
63739-724
Product ID
63739-724_99de73d1-2a10-4dab-b2da-b245b79452d6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210766
Marketing Start
2023-08-25
Marketing End
2026-07-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63739724
Hyphenated Format
63739-724
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA210766 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 meq/15mL
Packaging
- 5 TRAY in 1 CASE (63739-724-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (63739-724-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99de73d1-2a10-4dab-b2da-b245b79452d6", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["fc70ccc0-416e-4109-af22-6c6f00da5906"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 TRAY in 1 CASE (63739-724-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (63739-724-01)", "package_ndc": "63739-724-50", "marketing_end_date": "20260731", "marketing_start_date": "20230825"}], "brand_name": "Potassium Chloride", "product_id": "63739-724_99de73d1-2a10-4dab-b2da-b245b79452d6", "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": "63739-724", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA210766", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20230825"}