Home
>
National Drug Code (NDC)
>
Ciprofloxacin
Ciprofloxacin - 21695-914-40 - (Ciprofloxacin)
Drug Information of Ciprofloxacin
| Product NDC: | 21695-914 |
| Proprietary Name: | Ciprofloxacin |
| Non Proprietary Name: | Ciprofloxacin |
| Active Ingredient(s): | 400 mg/40mL & nbsp; Ciprofloxacin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin
| Product NDC: | 21695-914 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077245 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091208 |
Package Information of Ciprofloxacin
| Package NDC: | 21695-914-40 |
| Package Description: | 1 VIAL in 1 CARTON (21695-914-40) > 40 mL in 1 VIAL |
NDC Information of Ciprofloxacin
| NDC Code | 21695-914-40 |
| Proprietary Name | Ciprofloxacin |
| Package Description | 1 VIAL in 1 CARTON (21695-914-40) > 40 mL in 1 VIAL |
| Product NDC | 21695-914 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciprofloxacin |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091208 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CIPROFLOXACIN |
| Strength Number | 400 |
| Strength Unit | mg/40mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
