potassium chloride extended release (59917-103)

Drug Facts

Product Profile

Brand Name potassium chloride extended release

Generic Name potassium chloride

Labeler adare pharmaceuticals inc

Dosage Form CAPSULE

Routes

ORAL

Active Ingredients

potassium chloride 750 mg/1

Manufacturer

Adare Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 59917-103

Product ID 59917-103_0cf861f5-7a8c-9ba4-e063-6294a90a601f

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA208864

Listing Expiration 2026-12-31

Marketing Start 2018-04-01

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 59917103

Hyphenated Format 59917-103

Supplemental Identifiers

RxCUI

312504 315183

UPC

0359917103015 0359917102018

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 ANDA208864 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

750 mg/1

source: ndc

Packaging

100 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-01) / 1 CAPSULE in 1 CAPSULE
500 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-05) / 1 CAPSULE in 1 CAPSULE
1000 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-10) / 1 CAPSULE in 1 CAPSULE

source: ndc

Packages (3)

59917-103-01 100 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-01) / 1 CAPSULE in 1 CAPSULE 59917-103-05 500 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-05) / 1 CAPSULE in 1 CAPSULE 59917-103-10 1000 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-10) / 1 CAPSULE in 1 CAPSULE

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": "0cf861f5-7a8c-9ba4-e063-6294a90a601f", "openfda": {"upc": ["0359917103015", "0359917102018"], "unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["22edb0e6-4e45-4e91-aead-3581cca293a0"], "manufacturer_name": ["Adare Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-01)  / 1 CAPSULE in 1 CAPSULE", "package_ndc": "59917-103-01", "marketing_start_date": "20180401"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-05)  / 1 CAPSULE in 1 CAPSULE", "package_ndc": "59917-103-05", "marketing_start_date": "20180401"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (59917-103-10)  / 1 CAPSULE in 1 CAPSULE", "package_ndc": "59917-103-10", "marketing_start_date": "20180401"}], "brand_name": "POTASSIUM CHLORIDE EXTENDED RELEASE", "product_id": "59917-103_0cf861f5-7a8c-9ba4-e063-6294a90a601f", "dosage_form": "CAPSULE", "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": "59917-103", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Adare Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "brand_name_suffix": "EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA208864", "marketing_category": "ANDA", "marketing_start_date": "20180401", "listing_expiration_date": "20261231"}