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Abacavir Sulfate - 60505-3583-0 - (Abacavir Sulfate)

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Drug Information of Abacavir Sulfate

Product NDC: 60505-3583
Proprietary Name: Abacavir Sulfate
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 Sulfate

Product NDC: 60505-3583
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201570
Marketing Category: ANDA
Start Marketing Date: 20121217

Package Information of Abacavir Sulfate

Package NDC: 60505-3583-0
Package Description: 6 BLISTER PACK in 1 CARTON (60505-3583-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Abacavir Sulfate

NDC Code 60505-3583-0
Proprietary Name Abacavir Sulfate
Package Description 6 BLISTER PACK in 1 CARTON (60505-3583-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-3583
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Abacavir Sulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121217
Marketing Category Name ANDA
Labeler Name Apotex Corp
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 Sulfate


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