Didanosine - 54868-5464-0 - (Didanosine)

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Drug Information of Didanosine

Product NDC: 54868-5464
Proprietary Name: Didanosine
Non Proprietary Name: Didanosine
Active Ingredient(s): 250    mg/1 & nbsp;   Didanosine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of Didanosine

Product NDC: 54868-5464
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077167
Marketing Category: ANDA
Start Marketing Date: 20071213

Package Information of Didanosine

Package NDC: 54868-5464-0
Package Description: 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (54868-5464-0)

NDC Information of Didanosine

NDC Code 54868-5464-0
Proprietary Name Didanosine
Package Description 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (54868-5464-0)
Product NDC 54868-5464
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Didanosine
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 20071213
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DIDANOSINE
Strength Number 250
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