Package 60687-756-09

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 60687-756-09
Digits Only 6068775609
Product NDC 60687-756
Product ID 60687-756_384206f5-75c5-9bd2-e063-6294a90a5038
Description

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

Marketing

Marketing Status
Discontinued 2026-12-31
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": "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"}