sodium citrate and citric acid (81033-017)

Drug Facts

Product Profile

Brand Name sodium citrate and citric acid

Generic Name sodium citrate and citric acid

Labeler kesin pharma corporation

Dosage Form SOLUTION

Routes

ORAL

Active Ingredients

anhydrous citric acid 334 mg/5mL, sodium citrate 500 mg/5mL

Manufacturer

Kesin Pharma Corporation

Identifiers & Regulatory

Product NDC 81033-017

Product ID 81033-017_334a40cd-5521-39e3-e063-6394a90ab024

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category UNAPPROVED DRUG OTHER

Listing Expiration 2026-12-31

Marketing Start 2025-04-01

Pharmacologic Class

Established (EPC)

calculi dissolution agent [epc] anti-coagulant [epc]

Mechanism of Action

acidifying activity [moa] calcium chelating activity [moa]

Physiologic Effect

decreased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81033017

Hyphenated Format 81033-017

Supplemental Identifiers

RxCUI

543014

UNII

XF417D3PSL 1Q73Q2JULR

NUI

N0000175833 N0000175835 N0000175980 N0000008556 N0000175089

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 sodium citrate and citric acid (source: ndc)

Generic Name sodium citrate and citric acid (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

334 mg/5mL
500 mg/5mL

source: ndc

Packaging

100 CUP, UNIT-DOSE in 1 CASE (81033-017-50) / 15 mL in 1 CUP, UNIT-DOSE (81033-017-15)
100 CUP, UNIT-DOSE in 1 CASE (81033-017-51) / 30 mL in 1 CUP, UNIT-DOSE (81033-017-30)

source: ndc

Packages (2)

81033-017-50 100 CUP, UNIT-DOSE in 1 CASE (81033-017-50) / 15 mL in 1 CUP, UNIT-DOSE (81033-017-15) 81033-017-51 100 CUP, UNIT-DOSE in 1 CASE (81033-017-51) / 30 mL in 1 CUP, UNIT-DOSE (81033-017-30)

Ingredients (2)

anhydrous citric acid (334 mg/5mL) sodium citrate (500 mg/5mL)

Linked Drug Pages (1)

Sodium Citrate and Citric Acid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "334a40cd-5521-39e3-e063-6394a90ab024", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089"], "unii": ["XF417D3PSL", "1Q73Q2JULR"], "rxcui": ["543014"], "spl_set_id": ["3140f8fe-0644-7561-e063-6394a90a2c28"], "pharm_class_pe": ["Decreased Coagulation Factor Activity [PE]"], "pharm_class_epc": ["Calculi Dissolution Agent [EPC]", "Anti-coagulant [EPC]"], "pharm_class_moa": ["Acidifying Activity [MoA]", "Calcium Chelating Activity [MoA]"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-017-50)  / 15 mL in 1 CUP, UNIT-DOSE (81033-017-15)", "package_ndc": "81033-017-50", "marketing_start_date": "20250401"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-017-51)  / 30 mL in 1 CUP, UNIT-DOSE (81033-017-30)", "package_ndc": "81033-017-51", "marketing_start_date": "20250401"}], "brand_name": "Sodium Citrate and Citric Acid", "product_id": "81033-017_334a40cd-5521-39e3-e063-6394a90ab024", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "81033-017", "generic_name": "Sodium Citrate and Citric Acid", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Citrate and Citric Acid", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": "334 mg/5mL"}, {"name": "SODIUM CITRATE", "strength": "500 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}