sodium citrate and citric acid (60687-834)

Drug Facts

Product Profile

Brand Name sodium citrate and citric acid

Generic Name sodium citrate and citric acid monohydrate

Labeler american health packaging

Dosage Form SOLUTION

Routes

ORAL

Active Ingredients

anhydrous citric acid 2004 mg/30mL, sodium citrate, unspecified form 3000 mg/30mL

Manufacturer

American Health Packaging

Identifiers & Regulatory

Product NDC 60687-834

Product ID 60687-834_1d62bd0d-9703-cbc0-e063-6294a90a7eea

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category UNAPPROVED DRUG OTHER

Listing Expiration 2026-12-31

Marketing Start 2024-07-21

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 60687834

Hyphenated Format 60687-834

Supplemental Identifiers

RxCUI

543014

UNII

1Q73Q2JULR XF417D3PSL

NUI

N0000175833 N0000175835 N0000175980 N0000008556 N0000175089

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 sodium citrate and citric acid (source: ndc)

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

Routes

ORAL

source: ndc

Resolved Composition

Strengths

2004 mg/30mL
3000 mg/30mL

source: ndc

Packaging

10 TRAY in 1 CASE (60687-834-76) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-834-51) / 30 mL in 1 CUP, UNIT-DOSE (60687-834-45)

source: ndc

Packages (1)

60687-834-76 10 TRAY in 1 CASE (60687-834-76) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-834-51) / 30 mL in 1 CUP, UNIT-DOSE (60687-834-45)

Ingredients (2)

anhydrous citric acid (2004 mg/30mL) sodium citrate, unspecified form (3000 mg/30mL)

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": "1d62bd0d-9703-cbc0-e063-6294a90a7eea", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089"], "unii": ["1Q73Q2JULR", "XF417D3PSL"], "rxcui": ["543014"], "spl_set_id": ["58fa9952-c8ab-4ebb-a073-15cc45f4832a"], "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": ["American Health Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (60687-834-76)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-834-51)  / 30 mL in 1 CUP, UNIT-DOSE (60687-834-45)", "package_ndc": "60687-834-76", "marketing_start_date": "20240721"}], "brand_name": "Sodium Citrate and Citric Acid", "product_id": "60687-834_1d62bd0d-9703-cbc0-e063-6294a90a7eea", "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": "60687-834", "generic_name": "SODIUM CITRATE and CITRIC ACID MONOHYDRATE", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Citrate and Citric Acid", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": "2004 mg/30mL"}, {"name": "SODIUM CITRATE, UNSPECIFIED FORM", "strength": "3000 mg/30mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240721", "listing_expiration_date": "20261231"}