potassium chloride extended-release

Generic: potassium chloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride
Labeler american health packaging
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-632
Product ID 60687-632_204bc844-c945-938e-e063-6294a90ad011
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076368
Listing Expiration 2026-12-31
Marketing Start 2023-03-02

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 60687632
Hyphenated Format 60687-632

Supplemental Identifiers

RxCUI
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 (source: ndc)
Application Number ANDA076368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-632-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-632-11)
source: ndc

Packages (1)

60687-632-01 100 BLISTER PACK in 1 CARTON (60687-632-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-632-11)

Ingredients (1)

potassium chloride (750 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": "204bc844-c945-938e-e063-6294a90ad011", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["8c12c5f8-5950-44e3-9473-a0b95187b43c"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-632-01)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-632-11)", "package_ndc": "60687-632-01", "marketing_start_date": "20230302"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "60687-632_204bc844-c945-938e-e063-6294a90ad011", "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": "60687-632", "generic_name": "Potassium Chloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076368", "marketing_category": "ANDA", "marketing_start_date": "20230302", "listing_expiration_date": "20261231"}