potassium chloride
Generic: potassium chloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
potassium chloride 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-057
Product ID
72789-057_43d1320e-9de4-8602-e063-6294a90a9471
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208864
Listing Expiration
2026-12-31
Marketing Start
2020-01-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789057
Hyphenated Format
72789-057
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA208864 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-057-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43d1320e-9de4-8602-e063-6294a90a9471", "openfda": {"upc": ["0372789057309"], "unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["018fc687-1fba-202e-e063-6294a90a5c9a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-057-30)", "package_ndc": "72789-057-30", "marketing_start_date": "20230728"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "72789-057_43d1320e-9de4-8602-e063-6294a90a9471", "dosage_form": "CAPSULE, 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": "72789-057", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA208864", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}