potassium chloride extended-release (62207-727)

Drug Facts

Product Profile

Brand Name potassium chloride extended-release

Generic Name potassium chloride extended-release

Labeler granules india ltd

Dosage Form TABLET

Routes

ORAL

Active Ingredients

potassium chloride 1500 mg/1

Manufacturer

Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-727

Product ID 62207-727_44e29e92-b045-b2f8-e063-6394a90a7f6a

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA214452

Listing Expiration 2026-12-31

Marketing Start 2021-01-30

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 62207727

Hyphenated Format 62207-727

Supplemental Identifiers

RxCUI

1801294 1801298

UPC

0362207727495

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 extended-release (source: ndc)

Application Number ANDA214452 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

1500 mg/1

source: ndc

Packaging

800 TABLET in 1 BOTTLE (62207-727-08)
100 TABLET in 1 BOTTLE (62207-727-43)
500 TABLET in 1 BOTTLE (62207-727-47)
1000 TABLET in 1 BOTTLE (62207-727-49)
90 TABLET in 1 BOTTLE (62207-727-57)

source: ndc

Packages (5)

62207-727-08 800 TABLET in 1 BOTTLE (62207-727-08) 62207-727-43 100 TABLET in 1 BOTTLE (62207-727-43) 62207-727-47 500 TABLET in 1 BOTTLE (62207-727-47) 62207-727-49 1000 TABLET in 1 BOTTLE (62207-727-49) 62207-727-57 90 TABLET in 1 BOTTLE (62207-727-57)

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": "44e29e92-b045-b2f8-e063-6394a90a7f6a", "openfda": {"upc": ["0362207727495"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["60285a8d-bcb0-40ba-b359-df5c89480cd6"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "800 TABLET in 1 BOTTLE (62207-727-08)", "package_ndc": "62207-727-08", "marketing_start_date": "20210130"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62207-727-43)", "package_ndc": "62207-727-43", "marketing_start_date": "20210130"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62207-727-47)", "package_ndc": "62207-727-47", "marketing_start_date": "20210130"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62207-727-49)", "package_ndc": "62207-727-49", "marketing_start_date": "20210625"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62207-727-57)", "package_ndc": "62207-727-57", "marketing_start_date": "20210130"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "62207-727_44e29e92-b045-b2f8-e063-6394a90a7f6a", "dosage_form": "TABLET", "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": "62207-727", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Granules India Ltd", "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": "20210130", "listing_expiration_date": "20261231"}