Home
>
National Drug Code (NDC)
>
Ciprofloxacin
Ciprofloxacin - 68788-9944-5 - (Ciprofloxacin)
Drug Information of Ciprofloxacin
| Product NDC: | 68788-9944 |
| Proprietary Name: | Ciprofloxacin |
| Non Proprietary Name: | Ciprofloxacin |
| Active Ingredient(s): | 3 mg/mL & nbsp; Ciprofloxacin |
| Administration Route(s): | OPHTHALMIC; TOPICAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin
| Product NDC: | 68788-9944 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076673 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120112 |
Package Information of Ciprofloxacin
| Package NDC: | 68788-9944-5 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (68788-9944-5) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of Ciprofloxacin
| NDC Code | 68788-9944-5 |
| Proprietary Name | Ciprofloxacin |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (68788-9944-5) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 68788-9944 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciprofloxacin |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC; TOPICAL |
| Start Marketing Date | 20120112 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
