Rifampin - 51079-890-19 - (Rifampin)

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Drug Information of Rifampin

Product NDC: 51079-890
Proprietary Name: Rifampin
Non Proprietary Name: Rifampin
Active Ingredient(s): 300    mg/1 & nbsp;   Rifampin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Rifampin

Product NDC: 51079-890
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064150
Marketing Category: ANDA
Start Marketing Date: 20121205

Package Information of Rifampin

Package NDC: 51079-890-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-890-19) > 1 CAPSULE in 1 BLISTER PACK (51079-890-17)

NDC Information of Rifampin

NDC Code 51079-890-19
Proprietary Name Rifampin
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-890-19) > 1 CAPSULE in 1 BLISTER PACK (51079-890-17)
Product NDC 51079-890
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rifampin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121205
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name RIFAMPIN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Rifamycin Antibacterial [EPC],Rifamycins [Chemical/Ingredient]

Complete Information of Rifampin


General Information