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Theophylline - 29033-002-01 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 29033-002
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 600    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: 29033-002
Labeler Name: Nostrum Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040560
Marketing Category: ANDA
Start Marketing Date: 20070601

Package Information of Theophylline

Package NDC: 29033-002-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29033-002-01)

NDC Information of Theophylline

NDC Code 29033-002-01
Proprietary Name Theophylline
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29033-002-01)
Product NDC 29033-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070601
Marketing Category Name ANDA
Labeler Name Nostrum Laboratories, Inc.
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


General Information