NDC 55154-9419

Sodium Citrate and Citric Acid

Sodium Citrate And Citric Acid Monohydrate

Sodium Citrate and Citric Acid is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Cardinal Health. The primary component is Sodium Citrate, Unspecified Form; Anhydrous Citric Acid.

• Product ID: 55154-9419_67ceedaf-4f4a-4e9b-b5bd-ea2b4e33e7b5
• NDC: 55154-9419
• Product Type: Human Prescription Drug
• Proprietary Name: Sodium Citrate and Citric Acid
• Generic Name: Sodium Citrate And Citric Acid Monohydrate
• Dosage Form: Solution
• Route of Administration: ORAL
• Marketing Start Date: 1969-01-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Cardinal Health
• Substance Name: SODIUM CITRATE, UNSPECIFIED FORM; ANHYDROUS CITRIC ACID
• Active Ingredient Strength: 500 mg/5mL; mg/5mL
• Pharm Classes: Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 55154-9419-5

5 CUP, UNIT-DOSE in 1 BAG (55154-9419-5) > 15 mL in 1 CUP, UNIT-DOSE

• Marketing Start Date: 1969-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55154-9419-5 [55154941905]

Sodium Citrate and Citric Acid SOLUTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1969-01-01
• Marketing End Date: 2019-10-31

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM CITRATE, UNSPECIFIED FORM	500 mg/5mL

OpenFDA Data

• SPL SET ID: a7f42ce7-cc1c-43c4-acad-c95896a9a8c4
• Manufacturer:
  • Cardinal Health
• UNII:
  • XF417D3PSL
  • 1Q73Q2JULR
• RxNorm Concept Unique ID - RxCUI:
  • 543014

Pharmacological Class

• Acidifying Activity [MoA]
• Calculi Dissolution Agent [EPC]
• Anti-coagulant [EPC]
• Decreased Coagulation Factor Activity [PE]
• Calcium Chelating Activity [MoA]
• Acidifying Activity [MoA]
• Calculi Dissolution Agent [EPC]
• Anti-coagulant [EPC]
• Decreased Coagulation Factor Activity [PE]
• Calcium Chelating Activity [MoA]

NDC Crossover Matching brand name "Sodium Citrate and Citric Acid" or generic name "Sodium Citrate And Citric Acid Monohydrate"

NDC	Brand Name	Generic Name
0121-0595	Sodium Citrate and Citric Acid	SODIUM CITRATE and CITRIC ACID MONOHYDRATE
0121-1190	Sodium Citrate and Citric Acid	SODIUM CITRATE and CITRIC ACID MONOHYDRATE
17856-0595	Sodium Citrate and Citric Acid	SODIUM CITRATE and CITRIC ACID MONOHYDRATE
55154-5777	Sodium Citrate and Citric Acid	SODIUM CITRATE and CITRIC ACID MONOHYDRATE
55154-9410	Sodium Citrate and Citric Acid	SODIUM CITRATE and CITRIC ACID MONOHYDRATE
55154-9419	Sodium Citrate and Citric Acid	SODIUM CITRATE and CITRIC ACID MONOHYDRATE
62135-434	Sodium Citrate and Citric Acid	Sodium Citrate and Citric Acid
69367-320	Sodium Citrate and Citric Acid	sodium citrate and citric acid monohydrate