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Ciprofloxacin Otic
Ciprofloxacin Otic - 42195-550-14 - (CIPROFLOXACIN)
Drug Information of Ciprofloxacin Otic
| Product NDC: | 42195-550 |
| Proprietary Name: | Ciprofloxacin Otic |
| Non Proprietary Name: | CIPROFLOXACIN |
| Active Ingredient(s): | .5 mg/.25mL & nbsp; CIPROFLOXACIN |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin Otic
| Product NDC: | 42195-550 |
| Labeler Name: | Xspire Pharma |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021918 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120827 |
Package Information of Ciprofloxacin Otic
| Package NDC: | 42195-550-14 |
| Package Description: | 14 CONTAINER in 1 CARTON (42195-550-14) > .25 mL in 1 CONTAINER |
NDC Information of Ciprofloxacin Otic
| NDC Code | 42195-550-14 |
| Proprietary Name | Ciprofloxacin Otic |
| Package Description | 14 CONTAINER in 1 CARTON (42195-550-14) > .25 mL in 1 CONTAINER |
| Product NDC | 42195-550 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CIPROFLOXACIN |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20120827 |
| Marketing Category Name | NDA |
| Labeler Name | Xspire Pharma |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/.25mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
