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Ciprofloxacin
Ciprofloxacin - 0409-4765-86 - (CIPROFLOXACIN)
Drug Information of Ciprofloxacin
| Product NDC: | 0409-4765 |
| Proprietary Name: | Ciprofloxacin |
| Non Proprietary Name: | CIPROFLOXACIN |
| Active Ingredient(s): | 200 mg/20mL & nbsp; CIPROFLOXACIN |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin
| Product NDC: | 0409-4765 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077245 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060825 |
Package Information of Ciprofloxacin
| Package NDC: | 0409-4765-86 |
| Package Description: | 1 VIAL in 1 CARTON (0409-4765-86) > 20 mL in 1 VIAL |
NDC Information of Ciprofloxacin
| NDC Code | 0409-4765-86 |
| Proprietary Name | Ciprofloxacin |
| Package Description | 1 VIAL in 1 CARTON (0409-4765-86) > 20 mL in 1 VIAL |
| Product NDC | 0409-4765 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CIPROFLOXACIN |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20060825 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | CIPROFLOXACIN |
| Strength Number | 200 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
