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 CAPSULE, COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 10 meq/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-799
Product ID 68180-799_d5646d4c-67ac-4e51-85a9-cc8a6e60bebe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203002
Listing Expiration 2026-12-31
Marketing Start 2016-01-18

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 68180799
Hyphenated Format 68180-799

Supplemental Identifiers

RxCUI
312504 315183
UPC
0368180798019
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 ANDA203002 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-01)
  • 500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-02)
source: ndc

Packages (2)

68180-799-01 100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-01) 68180-799-02 500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-02)

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": "d5646d4c-67ac-4e51-85a9-cc8a6e60bebe", "openfda": {"upc": ["0368180798019"], "unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["1f33bcfe-c28a-4800-9241-685d974a5d91"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-01)", "package_ndc": "68180-799-01", "marketing_end_date": "20260430", "marketing_start_date": "20160525"}, {"sample": false, "description": "500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-02)", "package_ndc": "68180-799-02", "marketing_end_date": "20260430", "marketing_start_date": "20160304"}], "brand_name": "Potassium Chloride", "product_id": "68180-799_d5646d4c-67ac-4e51-85a9-cc8a6e60bebe", "dosage_form": "CAPSULE, COATED, 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": "68180-799", "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": "ANDA203002", "marketing_category": "ANDA", "marketing_start_date": "20160118", "listing_expiration_date": "20261231"}