potassium chloride extended-release

Generic: potassium chloride extended-release

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride extended-release
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8196
Product ID 68788-8196_bb1a06ef-f841-4688-97dc-b4cce0a19b06
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214452
Listing Expiration 2026-12-31
Marketing Start 2022-05-23

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 687888196
Hyphenated Format 68788-8196

Supplemental Identifiers

RxCUI
1801294
UNII
660YQ98I10

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
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-6)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-9)
source: ndc

Packages (3)

68788-8196-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-3) 68788-8196-6 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-6) 68788-8196-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-9)

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": "bb1a06ef-f841-4688-97dc-b4cce0a19b06", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["87f369cf-40e5-4f91-aa42-ae986fce6544"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-3)", "package_ndc": "68788-8196-3", "marketing_start_date": "20220523"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-6)", "package_ndc": "68788-8196-6", "marketing_start_date": "20220523"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-9)", "package_ndc": "68788-8196-9", "marketing_start_date": "20220523"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "68788-8196_bb1a06ef-f841-4688-97dc-b4cce0a19b06", "dosage_form": "TABLET, 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": "68788-8196", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20220523", "listing_expiration_date": "20261231"}