Product NDC: | 25021-132 |
Proprietary Name: | Levofloxacin |
Non Proprietary Name: | Levofloxacin |
Active Ingredient(s): | 5 mg/mL & nbsp; Levofloxacin |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 25021-132 |
Labeler Name: | Sagent Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090343 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110620 |
Package NDC: | 25021-132-82 |
Package Description: | 24 POUCH in 1 CARTON (25021-132-82) > 1 BAG in 1 POUCH > 100 mL in 1 BAG |
NDC Code | 25021-132-82 |
Proprietary Name | Levofloxacin |
Package Description | 24 POUCH in 1 CARTON (25021-132-82) > 1 BAG in 1 POUCH > 100 mL in 1 BAG |
Product NDC | 25021-132 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levofloxacin |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110620 |
Marketing Category Name | ANDA |
Labeler Name | Sagent Pharmaceuticals |
Substance Name | LEVOFLOXACIN |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |