potassium chloride

Generic: potassium chloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler avpak
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-671
Product ID 50268-671_43f8fa10-9261-a4f3-e063-6394a90a9e93
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202128
Listing Expiration 2026-12-31
Marketing Start 2016-01-28

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 50268671
Hyphenated Format 50268-671

Supplemental Identifiers

RxCUI
312504
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 ANDA202128 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-671-13) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-671-11)
source: ndc

Packages (1)

50268-671-13 30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-671-13) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-671-11)

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": "43f8fa10-9261-a4f3-e063-6394a90a9e93", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["6bb3f62d-79ce-cee6-8c6c-ee1eb6121f01"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-671-13)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-671-11)", "package_ndc": "50268-671-13", "marketing_start_date": "20160128"}], "brand_name": "Potassium Chloride", "product_id": "50268-671_43f8fa10-9261-a4f3-e063-6394a90a9e93", "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": "50268-671", "generic_name": "Potassium Chloride", "labeler_name": "AvPAK", "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": "20160128", "listing_expiration_date": "20261231"}