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Theophylline - 42858-701-01 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 42858-701
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 400    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: 42858-701
Labeler Name: Rhodes Pharmaceuticals L.P.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087571
Marketing Category: ANDA
Start Marketing Date: 20120202

Package Information of Theophylline

Package NDC: 42858-701-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42858-701-01)

NDC Information of Theophylline

NDC Code 42858-701-01
Proprietary Name Theophylline
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42858-701-01)
Product NDC 42858-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120202
Marketing Category Name ANDA
Labeler Name Rhodes Pharmaceuticals L.P.
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


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