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Theophylline - 55154-1345-0 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 55154-1345
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 300    mg/1 & nbsp;   Theophylline
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Theophylline

Product NDC: 55154-1345
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089763
Marketing Category: ANDA
Start Marketing Date: 20081113

Package Information of Theophylline

Package NDC: 55154-1345-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-1345-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Theophylline

NDC Code 55154-1345-0
Proprietary Name Theophylline
Package Description 10 BLISTER PACK in 1 BAG (55154-1345-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-1345
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20081113
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


General Information