potassium chloride

Generic: potassium chloride

Labeler: lupin pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler lupin pharmaceuticals,inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 40 meq/15mL

Manufacturer
Lupin Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 43386-169
Product ID 43386-169_b48fb85d-87f5-0c70-e053-2a95a90a7011
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209786
Listing Expiration 2026-12-31
Marketing Start 2018-09-24

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 43386169
Hyphenated Format 43386-169

Supplemental Identifiers

RxCUI
312515 314182
UPC
0343386169016 0343386168019
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 ANDA209786 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 meq/15mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (43386-169-01)
source: ndc

Packages (1)

43386-169-01 473 mL in 1 BOTTLE (43386-169-01)

Ingredients (1)

potassium chloride (40 meq/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": "b48fb85d-87f5-0c70-e053-2a95a90a7011", "openfda": {"upc": ["0343386169016", "0343386168019"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["28c49165-d8c9-443a-b000-953b8e1ec55c"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (43386-169-01)", "package_ndc": "43386-169-01", "marketing_start_date": "20180924"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "43386-169_b48fb85d-87f5-0c70-e053-2a95a90a7011", "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": "43386-169", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/15mL"}], "application_number": "ANDA209786", "marketing_category": "ANDA", "marketing_start_date": "20180924", "listing_expiration_date": "20261231"}