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Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride - 61314-656-05 - (Ciprofloxacin Hydrochloride)
Drug Information of Ciprofloxacin Hydrochloride
| Product NDC: | 61314-656 |
| Proprietary Name: | Ciprofloxacin Hydrochloride |
| Non Proprietary Name: | Ciprofloxacin Hydrochloride |
| Active Ingredient(s): | 3.5 mg/mL & nbsp; Ciprofloxacin Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin Hydrochloride
| Product NDC: | 61314-656 |
| Labeler Name: | Falcon Pharmaceuticals, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019992 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20040507 |
Package Information of Ciprofloxacin Hydrochloride
| Package NDC: | 61314-656-05 |
| Package Description: | 5 mL in 1 BOTTLE, PLASTIC (61314-656-05) |
NDC Information of Ciprofloxacin Hydrochloride
| NDC Code | 61314-656-05 |
| Proprietary Name | Ciprofloxacin Hydrochloride |
| Package Description | 5 mL in 1 BOTTLE, PLASTIC (61314-656-05) |
| Product NDC | 61314-656 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciprofloxacin Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20040507 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Falcon Pharmaceuticals, Ltd. |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 3.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
