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Ciprofloxacin - 16571-135-10 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 16571-135
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: 16571-135
Labeler Name: Pack Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077568
Marketing Category: ANDA
Start Marketing Date: 20100915

Package Information of Ciprofloxacin

Package NDC: 16571-135-10
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (16571-135-10) > 10 mL in 1 BOTTLE, PLASTIC

NDC Information of Ciprofloxacin

NDC Code 16571-135-10
Proprietary Name Ciprofloxacin
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (16571-135-10) > 10 mL in 1 BOTTLE, PLASTIC
Product NDC 16571-135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC; TOPICAL
Start Marketing Date 20100915
Marketing Category Name ANDA
Labeler Name Pack Pharmaceuticals, LLC
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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