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