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Theophylline - 68462-356-05 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 68462-356
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: 68462-356
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090355
Marketing Category: ANDA
Start Marketing Date: 20100713

Package Information of Theophylline

Package NDC: 68462-356-05
Package Description: 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-356-05)

NDC Information of Theophylline

NDC Code 68462-356-05
Proprietary Name Theophylline
Package Description 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-356-05)
Product NDC 68462-356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100713
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Theophylline


General Information