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Caffeine Citrate - 0574-0823-01 - (CAFFEINE CITRATE)

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Drug Information of Caffeine Citrate

Product NDC: 0574-0823
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
Coding System: National Drug Codes(NDC)

Labeler Information of Caffeine Citrate

Product NDC: 0574-0823
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077233
Marketing Category: ANDA
Start Marketing Date: 20060921

Package Information of Caffeine Citrate

Package NDC: 0574-0823-01
Package Description: 1 VIAL in 1 CARTON (0574-0823-01) > 3 mL in 1 VIAL

NDC Information of Caffeine Citrate

NDC Code 0574-0823-01
Proprietary Name Caffeine Citrate
Package Description 1 VIAL in 1 CARTON (0574-0823-01) > 3 mL in 1 VIAL
Product NDC 0574-0823
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CAFFEINE CITRATE
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20060921
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, 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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