| Product NDC: | 53808-0559 |
| Proprietary Name: | Rifampin |
| Non Proprietary Name: | RIFAMPIN |
| Active Ingredient(s): | 300 mg/1 & nbsp; RIFAMPIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53808-0559 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065028 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
| Package NDC: | 53808-0559-1 |
| Package Description: | 30 CAPSULE, COATED in 1 BLISTER PACK (53808-0559-1) |
| NDC Code | 53808-0559-1 |
| Proprietary Name | Rifampin |
| Package Description | 30 CAPSULE, COATED in 1 BLISTER PACK (53808-0559-1) |
| Product NDC | 53808-0559 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | RIFAMPIN |
| Dosage Form Name | CAPSULE, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | RIFAMPIN |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Rifamycin Antibacterial [EPC],Rifamycins [Chemical/Ingredient] |