NOROXIN - 0006-0705-20 - (Norfloxacin)

Alphabetical Index


Drug Information of NOROXIN

Product NDC: 0006-0705
Proprietary Name: NOROXIN
Non Proprietary Name: Norfloxacin
Active Ingredient(s): 400    mg/1 & nbsp;   Norfloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of NOROXIN

Product NDC: 0006-0705
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019384
Marketing Category: NDA
Start Marketing Date: 19861031

Package Information of NOROXIN

Package NDC: 0006-0705-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (0006-0705-20)

NDC Information of NOROXIN

NDC Code 0006-0705-20
Proprietary Name NOROXIN
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (0006-0705-20)
Product NDC 0006-0705
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norfloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19861031
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name NORFLOXACIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of NOROXIN


General Information