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Theophylline - 63629-2792-2 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 63629-2792
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 200    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: 63629-2792
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089808
Marketing Category: ANDA
Start Marketing Date: 20100913

Package Information of Theophylline

Package NDC: 63629-2792-2
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2792-2)

NDC Information of Theophylline

NDC Code 63629-2792-2
Proprietary Name Theophylline
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2792-2)
Product NDC 63629-2792
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100913
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


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