Product NDC: | 25021-130 |
Proprietary Name: | Levofloxacin |
Non Proprietary Name: | levofloxacin |
Active Ingredient(s): | 25 mg/mL & nbsp; levofloxacin |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 25021-130 |
Labeler Name: | Sagent Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA200560 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120105 |
Package NDC: | 25021-130-30 |
Package Description: | 1 VIAL in 1 CARTON (25021-130-30) > 30 mL in 1 VIAL |
NDC Code | 25021-130-30 |
Proprietary Name | Levofloxacin |
Package Description | 1 VIAL in 1 CARTON (25021-130-30) > 30 mL in 1 VIAL |
Product NDC | 25021-130 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | levofloxacin |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120105 |
Marketing Category Name | ANDA |
Labeler Name | Sagent Pharmaceuticals |
Substance Name | LEVOFLOXACIN |
Strength Number | 25 |
Strength Unit | mg/mL |
Pharmaceutical Classes |