potassium chloride extended-release

Generic: potassium chloride extended-release

Labeler: ncs healthcare of ky, llc dba vangard labs
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 ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8400
Product ID 0615-8400_aaf27061-fb9a-4a42-bc10-dec6a1304b18
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 06158400
Hyphenated Format 0615-8400

Supplemental Identifiers

RxCUI
1801294 1801298
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
  • 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8400-05)
  • 28 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8400-28)
  • 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8400-30) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8400-39)
source: ndc

Packages (4)

Ingredients (1)

potassium chloride (1500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aaf27061-fb9a-4a42-bc10-dec6a1304b18", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["c684758c-16f0-4bd9-b719-1aae64b7907f"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8400-05)", "package_ndc": "0615-8400-05", "marketing_start_date": "20210506"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8400-28)", "package_ndc": "0615-8400-28", "marketing_start_date": "20240502"}, {"sample": false, "description": "6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8400-30)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0615-8400-30", "marketing_start_date": "20210505"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8400-39)", "package_ndc": "0615-8400-39", "marketing_start_date": "20210506"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "0615-8400_aaf27061-fb9a-4a42-bc10-dec6a1304b18", "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": "0615-8400", "generic_name": "Potassium Chloride Extended-Release", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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"}