ACD - 14537-967-75 - (Dextrose Monohydrate, Sodium Citrate, and Anhydrous Citric Acid)

Alphabetical Index


Drug Information of ACD

Product NDC: 14537-967
Proprietary Name: ACD
Non Proprietary Name: Dextrose Monohydrate, Sodium Citrate, and Anhydrous Citric Acid
Active Ingredient(s): .73; 2.45; 2.2    g/100mL; g/100mL; g/100mL & nbsp;   Dextrose Monohydrate, Sodium Citrate, and Anhydrous Citric Acid
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ACD

Product NDC: 14537-967
Labeler Name: CaridianBCT, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA010228
Marketing Category: ANDA
Start Marketing Date: 20020225

Package Information of ACD

Package NDC: 14537-967-75
Package Description: 750 mL in 1 BAG (14537-967-75)

NDC Information of ACD

NDC Code 14537-967-75
Proprietary Name ACD
Package Description 750 mL in 1 BAG (14537-967-75)
Product NDC 14537-967
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextrose Monohydrate, Sodium Citrate, and Anhydrous Citric Acid
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20020225
Marketing Category Name ANDA
Labeler Name CaridianBCT, Inc.
Substance Name ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM CITRATE
Strength Number .73; 2.45; 2.2
Strength Unit g/100mL; g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of ACD


General Information