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Theophylline - 49349-010-02 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 49349-010
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 300    mg/1 & nbsp;   Theophylline
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Theophylline

Product NDC: 49349-010
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089763
Marketing Category: ANDA
Start Marketing Date: 20110707

Package Information of Theophylline

Package NDC: 49349-010-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-010-02)

NDC Information of Theophylline

NDC Code 49349-010-02
Proprietary Name Theophylline
Package Description 30 TABLET in 1 BLISTER PACK (49349-010-02)
Product NDC 49349-010
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110707
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name THEOPHYLLINE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


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