Product NDC: | 11673-403 |
Proprietary Name: | Motion Sickness Relief |
Non Proprietary Name: | Meclizine HCl |
Active Ingredient(s): | 25 mg/1 & nbsp; Meclizine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11673-403 |
Labeler Name: | Target Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part336 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20020624 |
Package NDC: | 11673-403-03 |
Package Description: | 10 TABLET in 1 VIAL, PLASTIC (11673-403-03) |
NDC Code | 11673-403-03 |
Proprietary Name | Motion Sickness Relief |
Package Description | 10 TABLET in 1 VIAL, PLASTIC (11673-403-03) |
Product NDC | 11673-403 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Meclizine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20020624 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Target Corporation |
Substance Name | MECLIZINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |