potassium chloride

Generic: potassium chloride

Labeler: granules india ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler granules india ltd
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-915
Product ID 62207-915_44f312e0-e1d8-5b18-e063-6294a90acc5e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214686
Listing Expiration 2026-12-31
Marketing Start 2023-01-01

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 62207915
Hyphenated Format 62207-915

Supplemental Identifiers

RxCUI
312504 315183
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 ANDA214686 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-43)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-47)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-49)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-57)
source: ndc

Packages (4)

62207-915-43 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-43) 62207-915-47 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-47) 62207-915-49 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-49) 62207-915-57 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-57)

Ingredients (1)

potassium chloride (750 mg/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": "44f312e0-e1d8-5b18-e063-6294a90acc5e", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["113c031c-6de3-4497-a57d-9740b1ce08ac"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-43)", "package_ndc": "62207-915-43", "marketing_start_date": "20230101"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-47)", "package_ndc": "62207-915-47", "marketing_start_date": "20230101"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-49)", "package_ndc": "62207-915-49", "marketing_start_date": "20230101"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62207-915-57)", "package_ndc": "62207-915-57", "marketing_start_date": "20230101"}], "brand_name": "Potassium Chloride", "product_id": "62207-915_44f312e0-e1d8-5b18-e063-6294a90acc5e", "dosage_form": "CAPSULE, 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": "62207-915", "generic_name": "Potassium Chloride", "labeler_name": "Granules India Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214686", "marketing_category": "ANDA", "marketing_start_date": "20230101", "listing_expiration_date": "20261231"}