potassium chloride

Generic: potassium chloride

Labeler: lupin limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

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 8 meq/1

Manufacturer
LUPIN LIMITED

Identifiers & Regulatory

Product NDC 57297-798
Product ID 57297-798_8ecf60cd-7ac7-46b2-93b5-19a8c274aec4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203002
Marketing Start 2016-05-25
Marketing End 2026-03-31

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 57297798
Hyphenated Format 57297-798

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
  • 8 meq/1
source: ndc
Packaging
  • 100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-798-01)
source: ndc

Packages (1)

57297-798-01 100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-798-01)

Ingredients (1)

potassium chloride (8 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 (57297-798-01)", "package_ndc": "57297-798-01", "marketing_end_date": "20260331", "marketing_start_date": "20160525"}], "brand_name": "Potassium Chloride", "product_id": "57297-798_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": "57297-798", "generic_name": "Potassium Chloride", "labeler_name": "LUPIN LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "8 meq/1"}], "application_number": "ANDA203002", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20160525"}