potassium chloride

Generic: potassium chloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 20 meq/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-365
Product ID 72789-365_3ba1064c-b041-c2b7-e063-6394a90ad3ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076368
Listing Expiration 2026-12-31
Marketing Start 2023-11-14

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 72789365
Hyphenated Format 72789-365

Supplemental Identifiers

RxCUI
1801294
UPC
0372789365305
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 ANDA076368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 meq/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-01)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-60)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-82)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-90)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-95)
source: ndc

Packages (6)

72789-365-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-01) 72789-365-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-30) 72789-365-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-60) 72789-365-82 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-82) 72789-365-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-90) 72789-365-95 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-95)

Ingredients (1)

potassium chloride (20 meq/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": "3ba1064c-b041-c2b7-e063-6394a90ad3ce", "openfda": {"upc": ["0372789365305"], "unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["47a87fb6-5e61-41c9-b759-10f7c74a67ce"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-01)", "package_ndc": "72789-365-01", "marketing_start_date": "20231204"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-30)", "package_ndc": "72789-365-30", "marketing_start_date": "20231228"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-60)", "package_ndc": "72789-365-60", "marketing_start_date": "20240119"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-82)", "package_ndc": "72789-365-82", "marketing_start_date": "20231114"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-90)", "package_ndc": "72789-365-90", "marketing_start_date": "20240119"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-95)", "package_ndc": "72789-365-95", "marketing_start_date": "20231228"}], "brand_name": "Potassium Chloride", "product_id": "72789-365_3ba1064c-b041-c2b7-e063-6394a90ad3ce", "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": "72789-365", "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": "20 meq/1"}], "application_number": "ANDA076368", "marketing_category": "ANDA", "marketing_start_date": "20231114", "listing_expiration_date": "20261231"}