potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 40 meq/15mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-495
Product ID 31722-495_7162658b-9e13-487e-bcf1-eda778fa3ac0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211992
Listing Expiration 2026-12-31
Marketing Start 2024-12-26

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 31722495
Hyphenated Format 31722-495

Supplemental Identifiers

RxCUI
312515 314182
UPC
0331722495479
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 ANDA211992 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 meq/15mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (31722-495-47)
source: ndc

Packages (1)

31722-495-47 473 mL in 1 BOTTLE, PLASTIC (31722-495-47)

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": "7162658b-9e13-487e-bcf1-eda778fa3ac0", "openfda": {"upc": ["0331722495479"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["fb2f6e74-4c1f-40c5-88a1-b88c069d4c75"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (31722-495-47)", "package_ndc": "31722-495-47", "marketing_start_date": "20241226"}], "brand_name": "Potassium chloride", "product_id": "31722-495_7162658b-9e13-487e-bcf1-eda778fa3ac0", "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": "31722-495", "generic_name": "potassium chloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/15mL"}], "application_number": "ANDA211992", "marketing_category": "ANDA", "marketing_start_date": "20241226", "listing_expiration_date": "20261231"}