potassium chloride (57297-799)

Drug Facts

Product Profile

Brand Name potassium chloride

Generic Name potassium chloride

Labeler lupin limited

Dosage Form CAPSULE, COATED, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

potassium chloride 10 meq/1

Manufacturer

LUPIN LIMITED

Identifiers & Regulatory

Product NDC 57297-799

Product ID 57297-799_8ecf60cd-7ac7-46b2-93b5-19a8c274aec4

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA203002

Marketing Start 2016-03-04

Marketing End 2026-04-30

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 57297799

Hyphenated Format 57297-799

Supplemental Identifiers

RxCUI

312504 315183

UPC

0368180798019

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 (source: ndc)

Generic Name potassium chloride (source: ndc)

Application Number ANDA203002 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

10 meq/1

source: ndc

Packaging

100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-01)
500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-02)
1000 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-03)

source: ndc

Packages (3)

57297-799-01 100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-01) 57297-799-02 500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-02) 57297-799-03 1000 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-03)

Ingredients (1)

potassium chloride (10 meq/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": "8ecf60cd-7ac7-46b2-93b5-19a8c274aec4", "openfda": {"upc": ["0368180798019"], "unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["56bb2200-da53-4f91-bdca-d76cc1ad6f8d"], "manufacturer_name": ["LUPIN LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-01)", "package_ndc": "57297-799-01", "marketing_end_date": "20260430", "marketing_start_date": "20160525"}, {"sample": false, "description": "500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-02)", "package_ndc": "57297-799-02", "marketing_end_date": "20260430", "marketing_start_date": "20160304"}, {"sample": false, "description": "1000 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-03)", "package_ndc": "57297-799-03", "marketing_end_date": "20260430", "marketing_start_date": "20160525"}], "brand_name": "Potassium Chloride", "product_id": "57297-799_8ecf60cd-7ac7-46b2-93b5-19a8c274aec4", "dosage_form": "CAPSULE, COATED, 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": "57297-799", "generic_name": "Potassium Chloride", "labeler_name": "LUPIN LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "10 meq/1"}], "application_number": "ANDA203002", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20160304"}