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CIPROFLOXACIN HYDROCHLORIDE
CIPROFLOXACIN HYDROCHLORIDE - 16590-421-05 - (CIPROFLOXACIN HYDROCHLORIDE)
Drug Information of CIPROFLOXACIN HYDROCHLORIDE
| Product NDC: | 16590-421 |
| 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: | 16590-421 |
| Labeler Name: | STAT Rx USA LLC |
| 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: | 16590-421-05 |
| Package Description: | 5 mL in 1 BOTTLE, PLASTIC (16590-421-05) |
NDC Information of CIPROFLOXACIN HYDROCHLORIDE
| NDC Code | 16590-421-05 |
| Proprietary Name | CIPROFLOXACIN HYDROCHLORIDE |
| Package Description | 5 mL in 1 BOTTLE, PLASTIC (16590-421-05) |
| Product NDC | 16590-421 |
| 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 | STAT Rx USA LLC |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 3.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
