Package 68084-850-32

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 68084-850-32
Digits Only 6808485032
Product NDC 68084-850
Product ID 68084-850_213c9f49-5d37-f84f-e063-6394a90aa698
Description

20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-850-32) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-850-33)

Marketing

Marketing Status
Marketed Since 2014-11-12
Brand potassium citrate
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

Potassium Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "213c9f49-5d37-f84f-e063-6394a90aa698", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["1201c777-2388-4235-bb8f-eb7dc1e867f8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-850-32)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-850-33)", "package_ndc": "68084-850-32", "marketing_start_date": "20141112"}], "brand_name": "Potassium Citrate", "product_id": "68084-850_213c9f49-5d37-f84f-e063-6394a90aa698", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "68084-850", "generic_name": "Potassium Citrate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA203546", "marketing_category": "ANDA", "marketing_start_date": "20141112", "listing_expiration_date": "20261231"}