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VIGAMOX
VIGAMOX - 21695-968-03 - (moxifloxacin hydrochloride)
Drug Information of VIGAMOX
| Product NDC: | 21695-968 |
| 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: | 21695-968 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021598 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030507 |
Package Information of VIGAMOX
| Package NDC: | 21695-968-03 |
| Package Description: | 3 mL in 1 BOTTLE, PLASTIC (21695-968-03) |
NDC Information of VIGAMOX
| NDC Code | 21695-968-03 |
| Proprietary Name | VIGAMOX |
| Package Description | 3 mL in 1 BOTTLE, PLASTIC (21695-968-03) |
| Product NDC | 21695-968 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | moxifloxacin hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20030507 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
