Product NDC: | 55150-156 |
Proprietary Name: | Levofloxacin |
Non Proprietary Name: | Levofloxacin |
Active Ingredient(s): | 500 mg/20mL & nbsp; Levofloxacin |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55150-156 |
Labeler Name: | AuroMedics Pharma LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA202328 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130124 |
Package NDC: | 55150-156-20 |
Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (55150-156-20) > 20 mL in 1 VIAL, SINGLE-USE |
NDC Code | 55150-156-20 |
Proprietary Name | Levofloxacin |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (55150-156-20) > 20 mL in 1 VIAL, SINGLE-USE |
Product NDC | 55150-156 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levofloxacin |
Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130124 |
Marketing Category Name | ANDA |
Labeler Name | AuroMedics Pharma LLC |
Substance Name | LEVOFLOXACIN |
Strength Number | 500 |
Strength Unit | mg/20mL |
Pharmaceutical Classes |