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Levofloxacin
Levofloxacin - 55648-547-01 - (Levofloxacin)
Drug Information of Levofloxacin
| Product NDC: | 55648-547 |
| 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: | 55648-547 |
| Labeler Name: | Wockhardt Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090367 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110620 |
Package Information of Levofloxacin
| Package NDC: | 55648-547-01 |
| Package Description: | 20 TABLET in 1 BOTTLE (55648-547-01) |
NDC Information of Levofloxacin
| NDC Code | 55648-547-01 |
| Proprietary Name | Levofloxacin |
| Package Description | 20 TABLET in 1 BOTTLE (55648-547-01) |
| Product NDC | 55648-547 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levofloxacin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110620 |
| Marketing Category Name | ANDA |
| Labeler Name | Wockhardt Limited |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
