NDC 0121-0595

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 Pharmaceutical Associates, Inc.. The primary component is Sodium Citrate; Anhydrous Citric Acid.

Product ID0121-0595_4bd10bd0-f555-11cd-e054-00144ff88e88
NDC0121-0595
Product TypeHuman Prescription Drug
Proprietary NameSodium Citrate and Citric Acid
Generic NameSodium Citrate And Citric Acid Monohydrate
Dosage FormSolution
Route of AdministrationORAL
Marketing Start Date1969-01-01
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NamePharmaceutical Associates, Inc.
Substance NameSODIUM CITRATE; ANHYDROUS CITRIC ACID
Active Ingredient Strength500 mg/5mL; mg/5mL
Pharm ClassesAcidifying 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 FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0121-0595-00

10 TRAY in 1 CASE (0121-0595-00) > 10 CUP, UNIT-DOSE in 1 TRAY > 15 mL in 1 CUP, UNIT-DOSE (0121-0595-15)
Marketing Start Date1969-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0121-0595-15 [00121059515]

Sodium Citrate and Citric Acid SOLUTION
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1969-01-01

NDC 0121-0595-30 [00121059530]

Sodium Citrate and Citric Acid SOLUTION
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1969-01-01

NDC 0121-0595-00 [00121059500]

Sodium Citrate and Citric Acid SOLUTION
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1969-01-01

NDC 0121-0595-16 [00121059516]

Sodium Citrate and Citric Acid SOLUTION
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1969-01-01

Drug Details

Active Ingredients

IngredientStrength
SODIUM CITRATE500 mg/5mL

OpenFDA Data

SPL SET ID:63201a61-6ac5-41ae-8b2d-ff0d3a8ddfd5
Manufacturer
UNII
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"

    NDCBrand NameGeneric Name
    0121-0595Sodium Citrate and Citric AcidSODIUM CITRATE and CITRIC ACID MONOHYDRATE
    0121-1190Sodium Citrate and Citric AcidSODIUM CITRATE and CITRIC ACID MONOHYDRATE
    17856-0595Sodium Citrate and Citric AcidSODIUM CITRATE and CITRIC ACID MONOHYDRATE
    55154-5777Sodium Citrate and Citric AcidSODIUM CITRATE and CITRIC ACID MONOHYDRATE
    55154-9410Sodium Citrate and Citric AcidSODIUM CITRATE and CITRIC ACID MONOHYDRATE
    55154-9419Sodium Citrate and Citric AcidSODIUM CITRATE and CITRIC ACID MONOHYDRATE
    62135-434Sodium Citrate and Citric AcidSodium Citrate and Citric Acid
    69367-320Sodium Citrate and Citric Acidsodium citrate and citric acid monohydrate

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