potassium citrate

Generic: potassium citrate

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium citrate
Generic Name potassium citrate
Labeler upsher-smith laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

potassium citrate 10 meq/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 0245-0071
Product ID 0245-0071_39e81850-ac5b-656e-e063-6294a90a1d94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019071
Marketing Start 2006-09-01
Marketing End 2027-07-31

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 02450071
Hyphenated Format 0245-0071

Supplemental Identifiers

RxCUI
199376 199381
UPC
0302450071112
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 potassium citrate (source: ndc)
Generic Name potassium citrate (source: ndc)
Application Number NDA019071 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0245-0071-11)
source: ndc

Packages (1)

0245-0071-11 100 TABLET in 1 BOTTLE (0245-0071-11)

Ingredients (1)

potassium citrate (10 meq/1)

Linked Drug Pages (1)

Potassium Citrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39e81850-ac5b-656e-e063-6294a90a1d94", "openfda": {"upc": ["0302450071112"], "unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381"], "spl_set_id": ["2215dc1d-0b5a-469e-9b51-4d7480a51078"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0245-0071-11)", "package_ndc": "0245-0071-11", "marketing_end_date": "20270731", "marketing_start_date": "20060901"}], "brand_name": "Potassium Citrate", "product_id": "0245-0071_39e81850-ac5b-656e-e063-6294a90a1d94", "dosage_form": "TABLET", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "0245-0071", "generic_name": "potassium citrate", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "NDA019071", "marketing_category": "NDA", "marketing_end_date": "20270731", "marketing_start_date": "20060901"}