Home
>
National Drug Code (NDC)
>
Ciprofloxacin and Dextrose
Ciprofloxacin and Dextrose - 0409-4777-49 - (CIPROFLOXACIN)
Drug Information of Ciprofloxacin and Dextrose
| Product NDC: | 0409-4777 |
| Proprietary Name: | Ciprofloxacin and Dextrose |
| Non Proprietary Name: | CIPROFLOXACIN |
| Active Ingredient(s): | 2 mg/mL & nbsp; CIPROFLOXACIN |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin and Dextrose
| Product NDC: | 0409-4777 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077753 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080318 |
Package Information of Ciprofloxacin and Dextrose
| Package NDC: | 0409-4777-49 |
| Package Description: | 24 BAG in 1 CASE (0409-4777-49) > 100 mL in 1 BAG |
NDC Information of Ciprofloxacin and Dextrose
| NDC Code | 0409-4777-49 |
| Proprietary Name | Ciprofloxacin and Dextrose |
| Package Description | 24 BAG in 1 CASE (0409-4777-49) > 100 mL in 1 BAG |
| Product NDC | 0409-4777 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CIPROFLOXACIN |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080318 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | CIPROFLOXACIN |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
