Home
>
National Drug Code (NDC)
>
Antivert
Antivert - 0049-2110-82 - (meclizine hydrochloride)
Drug Information of Antivert
| Product NDC: | 0049-2110 |
| Proprietary Name: | Antivert |
| Non Proprietary Name: | meclizine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; meclizine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antivert
| Product NDC: | 0049-2110 |
| Labeler Name: | Roerig |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA010721 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970411 |
Package Information of Antivert
| Package NDC: | 0049-2110-82 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0049-2110-82) |
NDC Information of Antivert
| NDC Code | 0049-2110-82 |
| Proprietary Name | Antivert |
| Package Description | 1000 TABLET in 1 BOTTLE (0049-2110-82) |
| Product NDC | 0049-2110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | meclizine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970411 |
| Marketing Category Name | NDA |
| Labeler Name | Roerig |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiemetic [EPC],Emesis Suppression [PE] |
