potassium chloride

Generic: potassium chloride

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler redpharm drug
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2131
Product ID 67296-2131_46ac9fcf-f297-e94a-e063-6294a90ab7ec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203562
Listing Expiration 2026-12-31
Marketing Start 2016-07-26

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 672962131
Hyphenated Format 67296-2131

Supplemental Identifiers

RxCUI
1801294
UPC
0368462471012 0368462472019
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 (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA203562 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2131-2)
source: ndc

Packages (1)

67296-2131-2 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2131-2)

Ingredients (1)

potassium chloride (1500 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": "46ac9fcf-f297-e94a-e063-6294a90ab7ec", "openfda": {"upc": ["0368462471012", "0368462472019"], "unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["3735d41a-7787-6b92-e063-6294a90add45"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2131-2)", "package_ndc": "67296-2131-2", "marketing_start_date": "20160726"}], "brand_name": "potassium chloride", "product_id": "67296-2131_46ac9fcf-f297-e94a-e063-6294a90ab7ec", "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": "67296-2131", "generic_name": "potassium chloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA203562", "marketing_category": "ANDA", "marketing_start_date": "20160726", "listing_expiration_date": "20261231"}