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Caffeine Citrate - 63323-407-03 - (CAFFEINE CITRATE)

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Drug Information of Caffeine Citrate

Product NDC: 63323-407
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: 63323-407
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077997
Marketing Category: ANDA
Start Marketing Date: 20091119

Package Information of Caffeine Citrate

Package NDC: 63323-407-03
Package Description: 1 VIAL in 1 BOX (63323-407-03) > 3 mL in 1 VIAL

NDC Information of Caffeine Citrate

NDC Code 63323-407-03
Proprietary Name Caffeine Citrate
Package Description 1 VIAL in 1 BOX (63323-407-03) > 3 mL in 1 VIAL
Product NDC 63323-407
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CAFFEINE CITRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091119
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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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