Didanosine - 0378-8889-93 - (didanosine enteric-coated beadlets)

Alphabetical Index


Drug Information of Didanosine

Product NDC: 0378-8889
Proprietary Name: Didanosine
Non Proprietary Name: didanosine enteric-coated beadlets
Active Ingredient(s): 400    mg/1 & nbsp;   didanosine enteric-coated beadlets
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Didanosine

Product NDC: 0378-8889
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090788
Marketing Category: ANDA
Start Marketing Date: 20120228

Package Information of Didanosine

Package NDC: 0378-8889-93
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-8889-93)

NDC Information of Didanosine

NDC Code 0378-8889-93
Proprietary Name Didanosine
Package Description 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-8889-93)
Product NDC 0378-8889
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name didanosine enteric-coated beadlets
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120228
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name DIDANOSINE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Didanosine


General Information