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Ciprofloxacin
Ciprofloxacin - 21695-422-01 - (Ciprofloxacin)
Drug Information of Ciprofloxacin
| Product NDC: | 21695-422 |
| Proprietary Name: | Ciprofloxacin |
| Non Proprietary Name: | Ciprofloxacin |
| Active Ingredient(s): | 10 mg/mL & nbsp; Ciprofloxacin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin
| Product NDC: | 21695-422 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077782 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060828 |
Package Information of Ciprofloxacin
| Package NDC: | 21695-422-01 |
| Package Description: | 20 mL in 1 VIAL (21695-422-01) |
NDC Information of Ciprofloxacin
| NDC Code | 21695-422-01 |
| Proprietary Name | Ciprofloxacin |
| Package Description | 20 mL in 1 VIAL (21695-422-01) |
| Product NDC | 21695-422 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciprofloxacin |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20060828 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CIPROFLOXACIN |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
