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Theophylline - 23155-063-03 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 23155-063
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 450    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: 23155-063
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090430
Marketing Category: ANDA
Start Marketing Date: 20101101

Package Information of Theophylline

Package NDC: 23155-063-03
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-063-03)

NDC Information of Theophylline

NDC Code 23155-063-03
Proprietary Name Theophylline
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-063-03)
Product NDC 23155-063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101101
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 450
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


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