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Ciprofloxacin - 52125-537-01 - (CIPROFLOXACIN HYDROCHLORIDE)

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Drug Information of Ciprofloxacin

Product NDC: 52125-537
Proprietary Name: Ciprofloxacin
Non Proprietary Name: CIPROFLOXACIN HYDROCHLORIDE
Active Ingredient(s): 3.5    mg/mL & nbsp;   CIPROFLOXACIN HYDROCHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 52125-537
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077689
Marketing Category: ANDA
Start Marketing Date: 20130423

Package Information of Ciprofloxacin

Package NDC: 52125-537-01
Package Description: 5 mL in 1 BOTTLE (52125-537-01)

NDC Information of Ciprofloxacin

NDC Code 52125-537-01
Proprietary Name Ciprofloxacin
Package Description 5 mL in 1 BOTTLE (52125-537-01)
Product NDC 52125-537
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CIPROFLOXACIN HYDROCHLORIDE
Dosage Form Name SOLUTION/ DROPS
Route Name TOPICAL
Start Marketing Date 20130423
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 3.5
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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