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CIPROFLOXACIN HYDROCHLORIDE - 16590-421-05 - (CIPROFLOXACIN HYDROCHLORIDE)

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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]

Complete Information of CIPROFLOXACIN HYDROCHLORIDE


General Information