potassium chloride extended release (0574-0275)

Drug Facts

Product Profile

Brand Name potassium chloride extended release

Generic Name potassium chloride

Labeler padagis us llc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

potassium chloride 750 mg/1

Manufacturer

Padagis US LLC

Identifiers & Regulatory

Product NDC 0574-0275

Product ID 0574-0275_f93209a4-1f6f-4b14-b707-dde758dbed2b

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA205993

Marketing Start 2015-12-11

Marketing End 2026-05-31

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 05740275

Hyphenated Format 0574-0275

Supplemental Identifiers

RxCUI

628953

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 extended release (source: ndc)

Generic Name potassium chloride (source: ndc)

Application Number ANDA205993 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

750 mg/1

source: ndc

Packaging

10 BLISTER PACK in 1 BOX, UNIT-DOSE (0574-0275-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (1)

0574-0275-11 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0574-0275-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

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": "f93209a4-1f6f-4b14-b707-dde758dbed2b", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["ef2f9647-00b5-439c-9ec6-2cbfe6bf3f3d"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (0574-0275-11)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0574-0275-11", "marketing_end_date": "20260531", "marketing_start_date": "20160505"}], "brand_name": "Potassium chloride extended release", "product_id": "0574-0275_f93209a4-1f6f-4b14-b707-dde758dbed2b", "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": "0574-0275", "generic_name": "Potassium chloride", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride extended release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA205993", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20151211"}