Home
>
National Drug Code (NDC)
>
Levofloxacin
Levofloxacin - 51079-034-20 - (levofloxacin)
Drug Information of Levofloxacin
| Product NDC: | 51079-034 |
| Proprietary Name: | Levofloxacin |
| Non Proprietary Name: | levofloxacin |
| Active Ingredient(s): | 250 mg/1 & nbsp; levofloxacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levofloxacin
| Product NDC: | 51079-034 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076276 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120827 |
Package Information of Levofloxacin
| Package NDC: | 51079-034-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-034-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-034-01) |
NDC Information of Levofloxacin
| NDC Code | 51079-034-20 |
| Proprietary Name | Levofloxacin |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-034-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-034-01) |
| Product NDC | 51079-034 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levofloxacin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120827 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional Inc. |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
