Rifampin - 0185-0799-30 - (Rifampin)

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Drug Information of Rifampin

Product NDC: 0185-0799
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: 0185-0799
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064150
Marketing Category: ANDA
Start Marketing Date: 19970528

Package Information of Rifampin

Package NDC: 0185-0799-30
Package Description: 30 CAPSULE in 1 BOTTLE (0185-0799-30)

NDC Information of Rifampin

NDC Code 0185-0799-30
Proprietary Name Rifampin
Package Description 30 CAPSULE in 1 BOTTLE (0185-0799-30)
Product NDC 0185-0799
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rifampin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970528
Marketing Category Name ANDA
Labeler Name Eon Labs, 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