RIFAMPIN - 68084-358-01 - (RIFAMPIN)

Alphabetical Index


Drug Information of RIFAMPIN

Product NDC: 68084-358
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: 68084-358
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065390
Marketing Category: ANDA
Start Marketing Date: 20090925

Package Information of RIFAMPIN

Package NDC: 68084-358-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-358-01) > 10 CAPSULE in 1 BLISTER PACK (68084-358-11)

NDC Information of RIFAMPIN

NDC Code 68084-358-01
Proprietary Name RIFAMPIN
Package Description 10 BLISTER PACK in 1 CARTON (68084-358-01) > 10 CAPSULE in 1 BLISTER PACK (68084-358-11)
Product NDC 68084-358
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RIFAMPIN
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090925
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name RIFAMPIN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Rifamycin Antibacterial [EPC],Rifamycins [Chemical/Ingredient]

Complete Information of RIFAMPIN


General Information