tricitrates

Generic: potassium citrate, sodium citrate, and citric acid monohydrate

Labeler: pai holdings, llc dba pai pharma
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name tricitrates
Generic Name potassium citrate, sodium citrate, and citric acid monohydrate
Labeler pai holdings, llc dba pai pharma
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

citric acid monohydrate 334 mg/5mL, potassium citrate 550 mg/5mL, sodium citrate 500 mg/5mL

Manufacturer
PAI Holdings, LLC dba PAI Pharma

Identifiers & Regulatory

Product NDC 0121-0677
Product ID 0121-0677_3082f36b-0006-4aee-9019-38995d2292fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2005-05-25

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 01210677
Hyphenated Format 0121-0677

Supplemental Identifiers

RxCUI
309317
UPC
0301210677168
UNII
2968PHW8QP EE90ONI6FF 1Q73Q2JULR

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 tricitrates (source: ndc)
Generic Name potassium citrate, sodium citrate, and citric acid monohydrate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 334 mg/5mL
  • 550 mg/5mL
  • 500 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (0121-0677-16)
source: ndc

Packages (1)

0121-0677-16 473 mL in 1 BOTTLE (0121-0677-16)

Ingredients (3)

citric acid monohydrate (334 mg/5mL) potassium citrate (550 mg/5mL) sodium citrate (500 mg/5mL)

Linked Drug Pages (1)

TRICITRATES ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3082f36b-0006-4aee-9019-38995d2292fd", "openfda": {"upc": ["0301210677168"], "unii": ["2968PHW8QP", "EE90ONI6FF", "1Q73Q2JULR"], "rxcui": ["309317"], "spl_set_id": ["2ecb42a2-82f1-456b-8f1e-02c2d0a7b5ad"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0121-0677-16)", "package_ndc": "0121-0677-16", "marketing_start_date": "20050525"}], "brand_name": "TRICITRATES", "product_id": "0121-0677_3082f36b-0006-4aee-9019-38995d2292fd", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "0121-0677", "generic_name": "POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRICITRATES", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "334 mg/5mL"}, {"name": "POTASSIUM CITRATE", "strength": "550 mg/5mL"}, {"name": "SODIUM CITRATE", "strength": "500 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20050525", "listing_expiration_date": "20261231"}