Product NDC: | 50383-286 |
Proprietary Name: | Levofloxacin |
Non Proprietary Name: | Levofloxacin |
Active Ingredient(s): | 25 mg/mL & nbsp; Levofloxacin |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50383-286 |
Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091678 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110621 |
Package NDC: | 50383-286-08 |
Package Description: | 1 BOTTLE in 1 CARTON (50383-286-08) > 200 mL in 1 BOTTLE |
NDC Code | 50383-286-08 |
Proprietary Name | Levofloxacin |
Package Description | 1 BOTTLE in 1 CARTON (50383-286-08) > 200 mL in 1 BOTTLE |
Product NDC | 50383-286 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levofloxacin |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20110621 |
Marketing Category Name | ANDA |
Labeler Name | Hi-Tech Pharmacal Co., Inc. |
Substance Name | LEVOFLOXACIN |
Strength Number | 25 |
Strength Unit | mg/mL |
Pharmaceutical Classes |