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levofloxacin
levofloxacin - 68788-9695-1 - (levofloxacin)
Drug Information of levofloxacin
| Product NDC: | 68788-9695 |
| 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: | 68788-9695 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090722 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130327 |
Package Information of levofloxacin
| Package NDC: | 68788-9695-1 |
| Package Description: | 10 TABLET in 1 BOTTLE (68788-9695-1) |
NDC Information of levofloxacin
| NDC Code | 68788-9695-1 |
| Proprietary Name | levofloxacin |
| Package Description | 10 TABLET in 1 BOTTLE (68788-9695-1) |
| Product NDC | 68788-9695 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levofloxacin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130327 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
