sodium citrate and citric acid

Generic: sodium citrate and citric acid monohydrate

Labeler: pharmaceutical associates, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name sodium citrate and citric acid
Generic Name sodium citrate and citric acid monohydrate
Labeler pharmaceutical associates, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

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

Manufacturer
Pharmaceutical Associates, Inc.

Identifiers & Regulatory

Product NDC 0121-1190
Product ID 0121-1190_26ce1be6-a69a-63f8-e063-6394a90ad637
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 1969-01-01

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 01211190
Hyphenated Format 0121-1190

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
  • 334 mg/5mL
  • 500 mg/5mL
source: ndc
Packaging
  • 10 TRAY in 1 CASE (0121-1190-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1190-30)
source: ndc

Packages (1)

0121-1190-00 10 TRAY in 1 CASE (0121-1190-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1190-30)

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": "26ce1be6-a69a-63f8-e063-6394a90ad637", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089"], "unii": ["1Q73Q2JULR", "XF417D3PSL"], "rxcui": ["543014"], "spl_set_id": ["63201a61-6ac5-41ae-8b2d-ff0d3a8ddfd5"], "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": ["Pharmaceutical Associates, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0121-1190-00)  / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1190-30)", "package_ndc": "0121-1190-00", "marketing_start_date": "19690101"}], "brand_name": "Sodium Citrate and Citric Acid", "product_id": "0121-1190_26ce1be6-a69a-63f8-e063-6394a90ad637", "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": "0121-1190", "generic_name": "SODIUM CITRATE and CITRIC ACID MONOHYDRATE", "labeler_name": "Pharmaceutical Associates, Inc.", "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": "19690101", "listing_expiration_date": "20261231"}