Abacavir - 68084-021-21 - (Abacavir Sulfate)

Alphabetical Index


Drug Information of Abacavir

Product NDC: 68084-021
Proprietary Name: Abacavir
Non Proprietary Name: Abacavir Sulfate
Active Ingredient(s): 300    mg/1 & nbsp;   Abacavir Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Abacavir

Product NDC: 68084-021
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077844
Marketing Category: ANDA
Start Marketing Date: 20130207

Package Information of Abacavir

Package NDC: 68084-021-21
Package Description: 3 BLISTER PACK in 1 CARTON (68084-021-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-021-11)

NDC Information of Abacavir

NDC Code 68084-021-21
Proprietary Name Abacavir
Package Description 3 BLISTER PACK in 1 CARTON (68084-021-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-021-11)
Product NDC 68084-021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Abacavir Sulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130207
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name ABACAVIR SULFATE
Strength Number 300
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 Abacavir


General Information