potassium citrate

Generic: potassium citrate

Labeler: biocomp pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name potassium citrate
Generic Name potassium citrate
Labeler biocomp pharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

potassium citrate 15 meq/1

Manufacturer
Biocomp Pharma, Inc.

Identifiers & Regulatory

Product NDC 44523-415
Product ID 44523-415_461546fa-70f8-dad0-e063-6394a90a4675
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA019071
Listing Expiration 2026-12-31
Marketing Start 2013-12-23

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 44523415
Hyphenated Format 44523-415

Supplemental Identifiers

RxCUI
199381 898490
UPC
0344523410015 0344523415010
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
  • 15 meq/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (44523-415-01)
source: ndc

Packages (1)

44523-415-01 100 TABLET in 1 BOTTLE (44523-415-01)

Ingredients (1)

potassium citrate (15 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": "461546fa-70f8-dad0-e063-6394a90a4675", "openfda": {"upc": ["0344523410015", "0344523415010"], "unii": ["EE90ONI6FF"], "rxcui": ["199381", "898490"], "spl_set_id": ["b32fe71a-4a58-04a1-64d3-bc3cc4a895bf"], "manufacturer_name": ["Biocomp Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (44523-415-01)", "package_ndc": "44523-415-01", "marketing_start_date": "20131223"}], "brand_name": "Potassium Citrate", "product_id": "44523-415_461546fa-70f8-dad0-e063-6394a90a4675", "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": "44523-415", "generic_name": "potassium citrate", "labeler_name": "Biocomp Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "15 meq/1"}], "application_number": "NDA019071", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20131223", "listing_expiration_date": "20261231"}