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Theophylline - 0904-5888-61 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 0904-5888
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: 0904-5888
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089808
Marketing Category: ANDA
Start Marketing Date: 20081113

Package Information of Theophylline

Package NDC: 0904-5888-61
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-5888-61)

NDC Information of Theophylline

NDC Code 0904-5888-61
Proprietary Name Theophylline
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-5888-61)
Product NDC 0904-5888
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 Major Pharmaceuticals
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


General Information