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Cipro
Cipro - 0085-1731-01 - (ciprofloxacin)
Drug Information of Cipro
| Product NDC: | 0085-1731 |
| Proprietary Name: | Cipro |
| Non Proprietary Name: | ciprofloxacin |
| Active Ingredient(s): | 10 mg/mL & nbsp; ciprofloxacin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cipro
| Product NDC: | 0085-1731 |
| Labeler Name: | Schering Plough Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019857 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090427 |
Package Information of Cipro
| Package NDC: | 0085-1731-01 |
| Package Description: | 40 mL in 1 VIAL, GLASS (0085-1731-01) |
NDC Information of Cipro
| NDC Code | 0085-1731-01 |
| Proprietary Name | Cipro |
| Package Description | 40 mL in 1 VIAL, GLASS (0085-1731-01) |
| Product NDC | 0085-1731 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin |
| Dosage Form Name | SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090427 |
| Marketing Category Name | NDA |
| Labeler Name | Schering Plough Corporation |
| Substance Name | CIPROFLOXACIN |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
