Home > National Drug Code (NDC) > Ciprofloxacin

Ciprofloxacin - 16571-120-50 - (CIPROFLOXACIN HYDROCHLORIDE)

Alphabetical Index


Drug Information of Ciprofloxacin

Product NDC: 16571-120
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: 16571-120
Labeler Name: PACK Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077689
Marketing Category: ANDA
Start Marketing Date: 20080320

Package Information of Ciprofloxacin

Package NDC: 16571-120-50
Package Description: 48 BOTTLE in 1 CASE (16571-120-50) > 5 mL in 1 BOTTLE

NDC Information of Ciprofloxacin

NDC Code 16571-120-50
Proprietary Name Ciprofloxacin
Package Description 48 BOTTLE in 1 CASE (16571-120-50) > 5 mL in 1 BOTTLE
Product NDC 16571-120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CIPROFLOXACIN HYDROCHLORIDE
Dosage Form Name SOLUTION/ DROPS
Route Name TOPICAL
Start Marketing Date 20080320
Marketing Category Name ANDA
Labeler Name PACK Pharmaceuticals, 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


General Information