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Theophylline - 49349-223-20 - (Theophylline)

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Drug Information of Theophylline

Product NDC: 49349-223
Proprietary Name: Theophylline
Non Proprietary Name: Theophylline
Active Ingredient(s): 200    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: 49349-223
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089808
Marketing Category: ANDA
Start Marketing Date: 20110427

Package Information of Theophylline

Package NDC: 49349-223-20
Package Description: 100 TABLET, EXTENDED RELEASE in 1 CANISTER (49349-223-20)

NDC Information of Theophylline

NDC Code 49349-223-20
Proprietary Name Theophylline
Package Description 100 TABLET, EXTENDED RELEASE in 1 CANISTER (49349-223-20)
Product NDC 49349-223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110427
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline


General Information