VIGAMOX - 54868-4798-0 - (moxifloxacin hydrochloride)

Alphabetical Index


Drug Information of VIGAMOX

Product NDC: 54868-4798
Proprietary Name: VIGAMOX
Non Proprietary Name: moxifloxacin hydrochloride
Active Ingredient(s): 5    mg/mL & nbsp;   moxifloxacin hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of VIGAMOX

Product NDC: 54868-4798
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021598
Marketing Category: NDA
Start Marketing Date: 20030522

Package Information of VIGAMOX

Package NDC: 54868-4798-0
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (54868-4798-0) > 3 mL in 1 BOTTLE, PLASTIC

NDC Information of VIGAMOX

NDC Code 54868-4798-0
Proprietary Name VIGAMOX
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (54868-4798-0) > 3 mL in 1 BOTTLE, PLASTIC
Product NDC 54868-4798
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name moxifloxacin hydrochloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20030522
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name MOXIFLOXACIN HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of VIGAMOX


General Information