Lufyllin - 0037-0731-92 - (Dyphylline)

Alphabetical Index


Drug Information of Lufyllin

Product NDC: 0037-0731
Proprietary Name: Lufyllin
Non Proprietary Name: Dyphylline
Active Ingredient(s): 400    mg/1 & nbsp;   Dyphylline
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lufyllin

Product NDC: 0037-0731
Labeler Name: Meda Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA084566
Marketing Category: NDA
Start Marketing Date: 19760831

Package Information of Lufyllin

Package NDC: 0037-0731-92
Package Description: 100 TABLET in 1 BOTTLE (0037-0731-92)

NDC Information of Lufyllin

NDC Code 0037-0731-92
Proprietary Name Lufyllin
Package Description 100 TABLET in 1 BOTTLE (0037-0731-92)
Product NDC 0037-0731
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dyphylline
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19760831
Marketing Category Name NDA
Labeler Name Meda Pharmaceuticals Inc.
Substance Name DYPHYLLINE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lufyllin


General Information