potassium chloride

Generic: potassium chloride

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler atlantic biologicals corp.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 3 g/15mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-1458
Product ID 17856-1458_35cf03f4-1fe9-5643-e063-6394a90a9e02
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210041
Listing Expiration 2026-12-31
Marketing Start 2018-07-24

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 178561458
Hyphenated Format 17856-1458

Supplemental Identifiers

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

Resolved Composition

Strengths
  • 3 g/15mL
source: ndc
Packaging
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1458-1) / 15 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (1)

17856-1458-1 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1458-1) / 15 mL in 1 CUP, UNIT-DOSE

Ingredients (1)

potassium chloride (3 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": "35cf03f4-1fe9-5643-e063-6394a90a9e02", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["314182"], "spl_set_id": ["104ccc91-2aaf-4bb7-bb64-77c29413f60e"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1458-1)  / 15 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-1458-1", "marketing_start_date": "20230920"}], "brand_name": "Potassium Chloride", "product_id": "17856-1458_35cf03f4-1fe9-5643-e063-6394a90a9e02", "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": "17856-1458", "generic_name": "Potassium Chloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "3 g/15mL"}], "application_number": "ANDA210041", "marketing_category": "ANDA", "marketing_start_date": "20180724", "listing_expiration_date": "20261231"}