potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 20 meq/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-756
Product ID 60687-756_384206f5-75c5-9bd2-e063-6294a90a5038
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075604
Marketing Start 2024-01-26
Marketing End 2026-12-31

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 60687756
Hyphenated Format 60687-756

Supplemental Identifiers

RxCUI
1801294
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 ANDA075604 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 meq/1
source: ndc
Packaging
  • 80 BLISTER PACK in 1 CARTON (60687-756-09) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-756-11)
source: ndc

Packages (1)

60687-756-09 80 BLISTER PACK in 1 CARTON (60687-756-09) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-756-11)

Ingredients (1)

potassium chloride (20 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": "384206f5-75c5-9bd2-e063-6294a90a5038", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["b165ad93-1dc1-4863-9f0b-d7b97c42c94c"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "80 BLISTER PACK in 1 CARTON (60687-756-09)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-756-11)", "package_ndc": "60687-756-09", "marketing_end_date": "20261231", "marketing_start_date": "20240126"}], "brand_name": "Potassium Chloride", "product_id": "60687-756_384206f5-75c5-9bd2-e063-6294a90a5038", "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": "60687-756", "generic_name": "Potassium Chloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/1"}], "application_number": "ANDA075604", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20240126"}