potassium chloride

Generic: potassium chloride

Labeler: amneal pharmaceuticals of new york llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler amneal pharmaceuticals of new york llc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Amneal Pharmaceuticals of New York LLC

Identifiers & Regulatory

Product NDC 53746-542
Product ID 53746-542_39798c58-3f69-43f2-b103-9da28abbeeba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202128
Listing Expiration 2026-12-31
Marketing Start 2013-02-22

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 53746542
Hyphenated Format 53746-542

Supplemental Identifiers

RxCUI
312504
UPC
0353746542014
UNII
660YQ98I10

Packaging Origin

Original Packager
true

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 ANDA202128 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-01)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-05)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-10)
source: ndc

Packages (3)

53746-542-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-01) 53746-542-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-05) 53746-542-10 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-10)

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": "39798c58-3f69-43f2-b103-9da28abbeeba", "openfda": {"upc": ["0353746542014"], "unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["cd56e147-92d6-46ce-ae00-63fac08d49b5"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-01)", "package_ndc": "53746-542-01", "marketing_start_date": "20130222"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-05)", "package_ndc": "53746-542-05", "marketing_start_date": "20130222"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53746-542-10)", "package_ndc": "53746-542-10", "marketing_start_date": "20130222"}], "brand_name": "Potassium Chloride", "product_id": "53746-542_39798c58-3f69-43f2-b103-9da28abbeeba", "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": "53746-542", "generic_name": "Potassium Chloride", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA202128", "marketing_category": "ANDA", "marketing_start_date": "20130222", "listing_expiration_date": "20261231"}