potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler lupin pharmaceuticals,inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 10 meq/1

Manufacturer
Lupin Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 43386-915
Product ID 43386-915_a056d531-3e7b-4598-a042-0d498456be72
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206347
Listing Expiration 2026-12-31
Marketing Start 2016-01-21

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 43386915
Hyphenated Format 43386-915

Supplemental Identifiers

RxCUI
1801294 1801298
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 ANDA206347 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-01)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-10)
source: ndc

Packages (2)

43386-915-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-01) 43386-915-10 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-10)

Ingredients (1)

potassium chloride (10 meq/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": "a056d531-3e7b-4598-a042-0d498456be72", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["fe08221d-74d5-490a-8db4-eaf3ed20b289"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-01)", "package_ndc": "43386-915-01", "marketing_start_date": "20160121"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-10)", "package_ndc": "43386-915-10", "marketing_start_date": "20170130"}], "brand_name": "Potassium Chloride", "product_id": "43386-915_a056d531-3e7b-4598-a042-0d498456be72", "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": "43386-915", "generic_name": "Potassium Chloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "10 meq/1"}], "application_number": "ANDA206347", "marketing_category": "ANDA", "marketing_start_date": "20160121", "listing_expiration_date": "20261231"}