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 SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/15mL

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-674
Product ID 50268-674_47fb4ce6-78ac-6467-e063-6294a90ace55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210041
Listing Expiration 2027-12-31
Marketing Start 2023-01-26

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 50268674
Hyphenated Format 50268-674

Supplemental Identifiers

RxCUI
312515 314182
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 ANDA210041 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/15mL
source: ndc
Packaging
  • 50 CUP in 1 BOX (50268-674-15) / 15 mL in 1 CUP (50268-674-11)
source: ndc

Packages (1)

50268-674-15 50 CUP in 1 BOX (50268-674-15) / 15 mL in 1 CUP (50268-674-11)

Ingredients (1)

potassium chloride (1.5 g/15mL)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47fb4ce6-78ac-6467-e063-6294a90ace55", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["f32df7c0-33eb-e6d6-e053-2a95a90a2e8d"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP in 1 BOX (50268-674-15)  / 15 mL in 1 CUP (50268-674-11)", "package_ndc": "50268-674-15", "marketing_start_date": "20230126"}], "brand_name": "Potassium Chloride", "product_id": "50268-674_47fb4ce6-78ac-6467-e063-6294a90ace55", "dosage_form": "SOLUTION", "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": "50268-674", "generic_name": "Potassium Chloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/15mL"}], "application_number": "ANDA210041", "marketing_category": "ANDA", "marketing_start_date": "20230126", "listing_expiration_date": "20271231"}