Home
>
National Drug Code (NDC)
>
Avelox
Avelox - 0085-1737-01 - (moxifloxacin hydrochloride)
Drug Information of Avelox
| Product NDC: | 0085-1737 |
| Proprietary Name: | Avelox |
| Non Proprietary Name: | moxifloxacin hydrochloride |
| Active Ingredient(s): | 400 mg/250mL & nbsp; moxifloxacin hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Avelox
| Product NDC: | 0085-1737 |
| Labeler Name: | Schering Plough Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021277 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20011130 |
Package Information of Avelox
| Package NDC: | 0085-1737-01 |
| Package Description: | 250 mL in 1 BAG (0085-1737-01) |
NDC Information of Avelox
| NDC Code | 0085-1737-01 |
| Proprietary Name | Avelox |
| Package Description | 250 mL in 1 BAG (0085-1737-01) |
| Product NDC | 0085-1737 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | moxifloxacin hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20011130 |
| Marketing Category Name | NDA |
| Labeler Name | Schering Plough Corporation |
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
| Strength Number | 400 |
| Strength Unit | mg/250mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
