Package 0178-0610-01

Brand: urocit-k

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 0178-0610-01
Digits Only 0178061001
Product NDC 0178-0610
Product ID 0178-0610_44ffdb97-c338-85b4-e063-6294a90a418a
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0610-01)

Marketing

Marketing Status
Marketed Since 2009-12-30
Brand urocit-k
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

UROCIT-K ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44ffdb97-c338-85b4-e063-6294a90a418a", "openfda": {"upc": ["0301780615010", "0301780600016", "0301780610015"], "unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381", "603281", "603282", "898490", "898517"], "spl_set_id": ["72cdea1b-2240-41db-987d-86d5c6aaa978"], "manufacturer_name": ["Mission Pharmacal Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0610-01)", "package_ndc": "0178-0610-01", "marketing_start_date": "20091230"}], "brand_name": "UROCIT-K", "product_id": "0178-0610_44ffdb97-c338-85b4-e063-6294a90a418a", "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": "0178-0610", "generic_name": "potassium citrate", "labeler_name": "Mission Pharmacal Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "UROCIT-K", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "NDA019071", "marketing_category": "NDA", "marketing_start_date": "19920901", "listing_expiration_date": "20261231"}