potassium chloride extended-release (70518-4383)

Drug Facts

Product Profile

Brand Name potassium chloride extended-release

Generic Name potassium chloride extended-release

Labeler remedyrepack inc.

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

potassium chloride 1500 mg/1

Manufacturer

REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4383

Product ID 70518-4383_450f7e33-d584-78ff-e063-6394a90a6333

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA214452

Listing Expiration 2026-12-31

Marketing Start 2025-07-02

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 705184383

Hyphenated Format 70518-4383

Supplemental Identifiers

RxCUI

1801294

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 extended-release (source: ndc)

Application Number ANDA214452 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

1500 mg/1

source: ndc

Packaging

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4383-0)
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4383-1)
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4383-2)

source: ndc

Packages (3)

70518-4383-0 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4383-0) 70518-4383-1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4383-1) 70518-4383-2 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4383-2)

Ingredients (1)

potassium chloride (1500 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": "450f7e33-d584-78ff-e063-6394a90a6333", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["ace1eb11-b925-405a-b772-58c60b3ca7d4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4383-0)", "package_ndc": "70518-4383-0", "marketing_start_date": "20250702"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4383-1)", "package_ndc": "70518-4383-1", "marketing_start_date": "20250724"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4383-2)", "package_ndc": "70518-4383-2", "marketing_start_date": "20251203"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "70518-4383_450f7e33-d584-78ff-e063-6394a90a6333", "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": "70518-4383", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20250702", "listing_expiration_date": "20261231"}