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Levofloxacin
Levofloxacin - 0143-9722-01 - (Levofloxacin)
Drug Information of Levofloxacin
| Product NDC: | 0143-9722 |
| Proprietary Name: | Levofloxacin |
| Non Proprietary Name: | Levofloxacin |
| Active Ingredient(s): | 250 mg/50mL & nbsp; Levofloxacin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levofloxacin
| Product NDC: | 0143-9722 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091375 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120131 |
Package Information of Levofloxacin
| Package NDC: | 0143-9722-01 |
| Package Description: | 24 POUCH in 1 CARTON (0143-9722-01) > 1 BAG in 1 POUCH > 50 mL in 1 BAG |
NDC Information of Levofloxacin
| NDC Code | 0143-9722-01 |
| Proprietary Name | Levofloxacin |
| Package Description | 24 POUCH in 1 CARTON (0143-9722-01) > 1 BAG in 1 POUCH > 50 mL in 1 BAG |
| Product NDC | 0143-9722 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levofloxacin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120131 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 250 |
| Strength Unit | mg/50mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
