Product NDC: | 63029-903 |
Proprietary Name: | Dramamine Less Drowsy |
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) |
Product NDC: | 63029-903 |
Labeler Name: | Medtech Products Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part336 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110901 |
Package NDC: | 63029-903-01 |
Package Description: | 1 BOTTLE in 1 BLISTER PACK (63029-903-01) > 8 TABLET in 1 BOTTLE |
NDC Code | 63029-903-01 |
Proprietary Name | Dramamine Less Drowsy |
Package Description | 1 BOTTLE in 1 BLISTER PACK (63029-903-01) > 8 TABLET in 1 BOTTLE |
Product NDC | 63029-903 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Meclizine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110901 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medtech Products Inc. |
Substance Name | MECLIZINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |