potassium chloride

Generic: potassium chloride

Labeler: glenmark pharmaceuticals inc., usa
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler glenmark pharmaceuticals inc., usa
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Glenmark Pharmaceuticals Inc., USA

Identifiers & Regulatory

Product NDC 68462-357
Product ID 68462-357_b0251572-aa7f-434a-a7ff-33ccbc37dfaf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202868
Listing Expiration 2026-12-31
Marketing Start 2016-01-20

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 68462357
Hyphenated Format 68462-357

Supplemental Identifiers

RxCUI
312504
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 ANDA202868 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-01)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-05)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-90)
source: ndc

Packages (3)

68462-357-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-01) 68462-357-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-05) 68462-357-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-90)

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": "b0251572-aa7f-434a-a7ff-33ccbc37dfaf", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["5b054142-7372-4641-be27-dca630a97ad9"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-01)", "package_ndc": "68462-357-01", "marketing_start_date": "20160120"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-05)", "package_ndc": "68462-357-05", "marketing_start_date": "20160120"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-90)", "package_ndc": "68462-357-90", "marketing_start_date": "20160601"}], "brand_name": "Potassium Chloride", "product_id": "68462-357_b0251572-aa7f-434a-a7ff-33ccbc37dfaf", "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": "68462-357", "generic_name": "Potassium Chloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA202868", "marketing_category": "ANDA", "marketing_start_date": "20160120", "listing_expiration_date": "20261231"}