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Theophylline - 54868-0029-7 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 54868-0029
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: 54868-0029
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089763
Marketing Category: ANDA
Start Marketing Date: 20070917

Package Information of Theophylline

Package NDC: 54868-0029-7
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-0029-7)

NDC Information of Theophylline

NDC Code 54868-0029-7
Proprietary Name Theophylline
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-0029-7)
Product NDC 54868-0029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070917
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


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