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Caffeine Citrate - 0517-0020-10 - (Caffeine Citrate)

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Drug Information of Caffeine Citrate

Product NDC: 0517-0020
Proprietary Name: Caffeine Citrate
Non Proprietary Name: Caffeine Citrate
Active Ingredient(s): 20    mg/mL & nbsp;   Caffeine Citrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Caffeine Citrate

Product NDC: 0517-0020
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077906
Marketing Category: ANDA
Start Marketing Date: 20070910

Package Information of Caffeine Citrate

Package NDC: 0517-0020-10
Package Description: 10 VIAL, SINGLE-DOSE in 1 TRAY (0517-0020-10) > 3 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Caffeine Citrate

NDC Code 0517-0020-10
Proprietary Name Caffeine Citrate
Package Description 10 VIAL, SINGLE-DOSE in 1 TRAY (0517-0020-10) > 3 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-0020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Caffeine Citrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070910
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name CAFFEINE CITRATE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Caffeine Citrate


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