Package 60687-810-09

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 60687-810-09
Digits Only 6068781009
Product NDC 60687-810
Product ID 60687-810_0f89e373-9a74-3bb0-e063-6294a90a65ee
Description

80 BLISTER PACK in 1 CARTON (60687-810-09) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-810-11)

Marketing

Marketing Status
Marketed Since 2024-01-20
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0f89e373-9a74-3bb0-e063-6294a90a65ee", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["a67f5ba7-ac23-4bdc-9563-cb7fd049a951"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "80 BLISTER PACK in 1 CARTON (60687-810-09)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-810-11)", "package_ndc": "60687-810-09", "marketing_start_date": "20240120"}], "brand_name": "Potassium Chloride", "product_id": "60687-810_0f89e373-9a74-3bb0-e063-6294a90a65ee", "dosage_form": "TABLET, FILM 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": "60687-810", "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": "750 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20240120", "listing_expiration_date": "20261231"}