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Motion Sickness Relief
Motion Sickness Relief - 41163-404-21 - (Meclizine HCl)
Drug Information of Motion Sickness Relief
| Product NDC: | 41163-404 |
| 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, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Motion Sickness Relief
| Product NDC: | 41163-404 |
| Labeler Name: | SUPERVALU INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20020529 |
Package Information of Motion Sickness Relief
| Package NDC: | 41163-404-21 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (41163-404-21) > 16 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Information of Motion Sickness Relief
| NDC Code | 41163-404-21 |
| Proprietary Name | Motion Sickness Relief |
| Package Description | 1 BLISTER PACK in 1 CARTON (41163-404-21) > 16 TABLET, CHEWABLE in 1 BLISTER PACK |
| Product NDC | 41163-404 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Meclizine HCl |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20020529 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SUPERVALU INC. |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
