VIGAMOX is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is Moxifloxacin Hydrochloride.
Product ID | 0065-4013_0781161f-3088-4721-ad72-c7daeb88fc58 |
NDC | 0065-4013 |
Product Type | Human Prescription Drug |
Proprietary Name | VIGAMOX |
Generic Name | Moxifloxacin Hydrochloride |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 2003-05-07 |
Marketing End Date | 2022-07-31 |
Marketing Category | NDA / NDA |
Application Number | NDA021598 |
Labeler Name | Alcon Laboratories, Inc. |
Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
Active Ingredient Strength | 5 mg/mL |
Pharm Classes | Quinolone Antimicrobial [EPC], Quinolones [CS] |
NDC Exclude Flag | N |
Marketing Start Date | 2003-05-07 |
Marketing End Date | 2022-07-31 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021598 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2003-05-07 |
Marketing Category | NDA |
Application Number | NDA021598 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2003-05-07 |
Marketing Category | NDA |
Application Number | NDA021598 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2003-05-07 |
Marketing End Date | 2011-07-14 |
Ingredient | Strength |
---|---|
MOXIFLOXACIN HYDROCHLORIDE | 5 mg/mL |
SPL SET ID: | 0e6ab6ba-5eeb-4faf-ba80-4bf21a74228a |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0065-4013 | VIGAMOX | moxifloxacin hydrochloride |
0078-0939 | VIGAMOX | moxifloxacin hydrochloride |
21695-968 | VIGAMOX | moxifloxacin hydrochloride |
50090-0859 | VIGAMOX | moxifloxacin hydrochloride |
70518-2043 | VIGAMOX | VIGAMOX |
0085-1733 | Avelox | moxifloxacin hydrochloride |
0085-1737 | Avelox | moxifloxacin hydrochloride |
0065-0006 | MOXEZA | moxifloxacin hydrochloride |
48792-7823 | Moxifloxacin | moxifloxacin hydrochloride |
0093-7387 | Moxifloxacin Hydrochloride | Moxifloxacin Hydrochloride |
0832-1410 | Moxifloxacin Hydrochloride | Moxifloxacin Hydrochloride |
13668-201 | moxifloxacin hydrochloride | moxifloxacin hydrochloride |
40032-034 | Moxifloxacin Hydrochloride | Moxifloxacin Hydrochloride |
43063-580 | Moxifloxacin Hydrochloride | moxifloxacin hydrochloride |
43063-585 | Moxifloxacin Hydrochloride | moxifloxacin hydrochloride |
47781-268 | Moxifloxacin Hydrochloride | moxifloxacin hydrochloride |
50090-4058 | Moxifloxacin Hydrochloride | Moxifloxacin Hydrochloride |
50090-4100 | Moxifloxacin Hydrochloride | Moxifloxacin Hydrochloride |
0781-7135 | Moxifloxacin Ophthalmic Solution | moxifloxacin hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VIGAMOX 78203609 2924187 Live/Registered |
NOVARTIS AG 2003-01-15 |
VIGAMOX 77770376 3751687 Live/Registered |
NOVARTIS AG 2009-06-29 |