potassium chloride

Generic: potassium chloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler major pharmaceuticals
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7292
Product ID 0904-7292_7e4c4d5e-c399-4985-af8f-0be1177fa380
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212861
Marketing Start 2023-05-01
Marketing End 2026-06-30

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 09047292
Hyphenated Format 0904-7292

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 ANDA212861 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7292-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7292-61 100 BLISTER PACK in 1 CARTON (0904-7292-61) / 1 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": "7e4c4d5e-c399-4985-af8f-0be1177fa380", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["7c2274f2-5a7f-4a4a-8b7b-44f6ef9a84a4"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7292-61)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-7292-61", "marketing_end_date": "20260630", "marketing_start_date": "20230501"}], "brand_name": "Potassium Chloride", "product_id": "0904-7292_7e4c4d5e-c399-4985-af8f-0be1177fa380", "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": "0904-7292", "generic_name": "Potassium Chloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA212861", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20230501"}