Theo-24 - 50474-400-01 - (theophylline anhydrous)

Alphabetical Index


Drug Information of Theo-24

Product NDC: 50474-400
Proprietary Name: Theo-24
Non Proprietary Name: theophylline anhydrous
Active Ingredient(s): 400    mg/1 & nbsp;   theophylline anhydrous
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Theo-24

Product NDC: 50474-400
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081034
Marketing Category: ANDA
Start Marketing Date: 19980109

Package Information of Theo-24

Package NDC: 50474-400-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-400-01)

NDC Information of Theo-24

NDC Code 50474-400-01
Proprietary Name Theo-24
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-400-01)
Product NDC 50474-400
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name theophylline anhydrous
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19980109
Marketing Category Name ANDA
Labeler Name UCB, Inc.
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theo-24


General Information