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LEVAQUIN
LEVAQUIN - 50458-164-20 - (levofloxacin)
Drug Information of LEVAQUIN
| Product NDC: | 50458-164 |
| Proprietary Name: | LEVAQUIN |
| Non Proprietary Name: | levofloxacin |
| Active Ingredient(s): | 25 mg/mL & nbsp; levofloxacin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVAQUIN
| Product NDC: | 50458-164 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020635 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961220 |
Package Information of LEVAQUIN
| Package NDC: | 50458-164-20 |
| Package Description: | 20 mL in 1 VIAL, SINGLE-USE (50458-164-20) |
NDC Information of LEVAQUIN
| NDC Code | 50458-164-20 |
| Proprietary Name | LEVAQUIN |
| Package Description | 20 mL in 1 VIAL, SINGLE-USE (50458-164-20) |
| Product NDC | 50458-164 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levofloxacin |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19961220 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
