urocit-k

Generic: potassium citrate

Labeler: mission pharmacal company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name urocit-k
Generic Name potassium citrate
Labeler mission pharmacal company
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium citrate 15 meq/1

Manufacturer
Mission Pharmacal Company

Identifiers & Regulatory

Product NDC 0178-0615
Product ID 0178-0615_44ffdb97-c338-85b4-e063-6294a90a418a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019071
Listing Expiration 2026-12-31
Marketing Start 2010-01-27

Pharmacologic Class

Classes
acidifying activity [moa] anti-coagulant [epc] calcium chelating activity [moa] calculi dissolution agent [epc] decreased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01780615
Hyphenated Format 0178-0615

Supplemental Identifiers

RxCUI
199376 199381 603281 603282 898490 898517
UPC
0301780615010 0301780600016 0301780610015
UNII
EE90ONI6FF

Packaging Origin

Original Packager
true

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 urocit-k (source: ndc)
Generic Name potassium citrate (source: ndc)
Application Number NDA019071 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 meq/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0615-01)
source: ndc

Packages (1)

0178-0615-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0615-01)

Ingredients (1)

potassium citrate (15 meq/1)

Linked Drug Pages (1)

UROCIT-K ndc-match (0.9)

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 (0178-0615-01)", "package_ndc": "0178-0615-01", "marketing_start_date": "20100127"}], "brand_name": "UROCIT-K", "product_id": "0178-0615_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": "0178-0615", "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": "15 meq/1"}], "application_number": "NDA019071", "marketing_category": "NDA", "marketing_start_date": "20100127", "listing_expiration_date": "20261231"}