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Theophylline - 53808-0316-1 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 53808-0316
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 300    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: 53808-0316
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089763
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Theophylline

Package NDC: 53808-0316-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (53808-0316-1)

NDC Information of Theophylline

NDC Code 53808-0316-1
Proprietary Name Theophylline
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (53808-0316-1)
Product NDC 53808-0316
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


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