potassium chloride extended-release

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride
Labeler remedyrepack inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3024
Product ID 70518-3024_4b0734d3-4447-dbd5-e063-6394a90ae2b1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076368
Listing Expiration 2027-12-31
Marketing Start 2021-02-15

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 705183024
Hyphenated Format 70518-3024

Supplemental Identifiers

RxCUI
1801298
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 extended-release (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA076368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3024-1)
source: ndc

Packages (1)

70518-3024-1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3024-1)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b0734d3-4447-dbd5-e063-6394a90ae2b1", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["7ec22e8e-6643-44fe-804d-ca0b0b266663"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3024-1)", "package_ndc": "70518-3024-1", "marketing_start_date": "20250621"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "70518-3024_4b0734d3-4447-dbd5-e063-6394a90ae2b1", "dosage_form": "TABLET, 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": "70518-3024", "generic_name": "Potassium Chloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076368", "marketing_category": "ANDA", "marketing_start_date": "20210215", "listing_expiration_date": "20271231"}