Home
>
National Drug Code (NDC)
>
Levofloxacin
Levofloxacin - 68788-9709-2 - (Levofloxacin)
Drug Information of Levofloxacin
| Product NDC: | 68788-9709 |
| Proprietary Name: | Levofloxacin |
| Non Proprietary Name: | Levofloxacin |
| Active Ingredient(s): | 750 mg/1 & nbsp; Levofloxacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levofloxacin
| Product NDC: | 68788-9709 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090367 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130204 |
Package Information of Levofloxacin
| Package NDC: | 68788-9709-2 |
| Package Description: | 20 TABLET in 1 BOTTLE (68788-9709-2) |
NDC Information of Levofloxacin
| NDC Code | 68788-9709-2 |
| Proprietary Name | Levofloxacin |
| Package Description | 20 TABLET in 1 BOTTLE (68788-9709-2) |
| Product NDC | 68788-9709 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levofloxacin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130204 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
