Mycobutin - 54868-2841-4 - (rifabutin)

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Drug Information of Mycobutin

Product NDC: 54868-2841
Proprietary Name: Mycobutin
Non Proprietary Name: rifabutin
Active Ingredient(s): 150    mg/1 & nbsp;   rifabutin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Mycobutin

Product NDC: 54868-2841
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050689
Marketing Category: NDA
Start Marketing Date: 19950315

Package Information of Mycobutin

Package NDC: 54868-2841-4
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-2841-4)

NDC Information of Mycobutin

NDC Code 54868-2841-4
Proprietary Name Mycobutin
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-2841-4)
Product NDC 54868-2841
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rifabutin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950315
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name RIFABUTIN
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Rifamycin Antimycobacterial [EPC],Rifamycins [Chemical/Ingredient]

Complete Information of Mycobutin


General Information