potassium chloride

Generic: potassium chloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

potassium chloride 750 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4050
Product ID 70518-4050_3fa16c36-fa12-db93-e063-6394a90ad2bf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214686
Listing Expiration 2026-12-31
Marketing Start 2024-04-11

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 705184050
Hyphenated Format 70518-4050

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 ANDA214686 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4050-0)
  • 100 POUCH in 1 BOX (70518-4050-1) / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-4050-2)
source: ndc

Packages (2)

70518-4050-0 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4050-0) 70518-4050-1 100 POUCH in 1 BOX (70518-4050-1) / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-4050-2)

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": "3fa16c36-fa12-db93-e063-6394a90ad2bf", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["f75713cf-6902-4160-94cb-335a1ecdbbbe"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4050-0)", "package_ndc": "70518-4050-0", "marketing_start_date": "20240411"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-4050-1)  / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-4050-2)", "package_ndc": "70518-4050-1", "marketing_start_date": "20240615"}], "brand_name": "Potassium Chloride", "product_id": "70518-4050_3fa16c36-fa12-db93-e063-6394a90ad2bf", "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": "70518-4050", "generic_name": "Potassium Chloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214686", "marketing_category": "ANDA", "marketing_start_date": "20240411", "listing_expiration_date": "20261231"}