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Rifampin
Rifampin - 0185-0799-30 - (Rifampin)
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] |
