Home
>
National Drug Code (NDC)
>
Ciprofloxacin
Ciprofloxacin - 0781-3239-09 - (Ciprofloxacin)
Drug Information of Ciprofloxacin
| Product NDC: | 0781-3239 |
| Proprietary Name: | Ciprofloxacin |
| Non Proprietary Name: | Ciprofloxacin |
| Active Ingredient(s): | 2 mg/mL & nbsp; Ciprofloxacin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin
| Product NDC: | 0781-3239 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078252 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080324 |
Package Information of Ciprofloxacin
| Package NDC: | 0781-3239-09 |
| Package Description: | 24 POUCH in 1 CARTON (0781-3239-09) > 1 BAG in 1 POUCH (0781-3239-46) > 100 mL in 1 BAG |
NDC Information of Ciprofloxacin
| NDC Code | 0781-3239-09 |
| Proprietary Name | Ciprofloxacin |
| Package Description | 24 POUCH in 1 CARTON (0781-3239-09) > 1 BAG in 1 POUCH (0781-3239-46) > 100 mL in 1 BAG |
| Product NDC | 0781-3239 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciprofloxacin |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080324 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CIPROFLOXACIN |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
