potassium chloride

Generic: potassium chloride

Labeler: advagen pharma ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler advagen pharma ltd.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Advagen Pharma Ltd.

Identifiers & Regulatory

Product NDC 72888-097
Product ID 72888-097_47c7b555-0f26-f6ff-e063-6294a90a05ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216321
Listing Expiration 2027-12-31
Marketing Start 2023-06-16

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 72888097
Hyphenated Format 72888-097

Supplemental Identifiers

RxCUI
403888 1801294 1801298
UPC
0372888098012 0372888099002 0372888097008 0372888097015 0372888098005 0372888099019
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 ANDA216321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-00)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-01)
source: ndc

Packages (2)

72888-097-00 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-00) 72888-097-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-01)

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": "47c7b555-0f26-f6ff-e063-6294a90a05ce", "openfda": {"upc": ["0372888098012", "0372888099002", "0372888097008", "0372888097015", "0372888098005", "0372888099019"], "unii": ["660YQ98I10"], "rxcui": ["403888", "1801294", "1801298"], "spl_set_id": ["f4497c26-da16-45b0-975d-81f2c2132704"], "manufacturer_name": ["Advagen Pharma Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-00)", "package_ndc": "72888-097-00", "marketing_start_date": "20230616"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-01)", "package_ndc": "72888-097-01", "marketing_start_date": "20230616"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "72888-097_47c7b555-0f26-f6ff-e063-6294a90a05ce", "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": "72888-097", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Advagen Pharma Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA216321", "marketing_category": "ANDA", "marketing_start_date": "20230616", "listing_expiration_date": "20271231"}