Home > National Drug Code (NDC) > Ciprofloxacin

Ciprofloxacin - 49999-699-05 - (Ciprofloxacin)

Alphabetical Index


Drug Information of Ciprofloxacin

Product NDC: 49999-699
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 3    mg/mL & nbsp;   Ciprofloxacin
Administration Route(s): OPHTHALMIC; TOPICAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 49999-699
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076673
Marketing Category: ANDA
Start Marketing Date: 20050121

Package Information of Ciprofloxacin

Package NDC: 49999-699-05
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (49999-699-05) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Ciprofloxacin

NDC Code 49999-699-05
Proprietary Name Ciprofloxacin
Package Description 1 BOTTLE, DROPPER in 1 CARTON (49999-699-05) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 49999-699
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC; TOPICAL
Start Marketing Date 20050121
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


General Information