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Motion sickness
Motion sickness - 49348-363-67 - (Meclizine HCl)
Drug Information of Motion sickness
| Product NDC: | 49348-363 |
| Proprietary Name: | Motion sickness |
| 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) |
Labeler Information of Motion sickness
| Product NDC: | 49348-363 |
| Labeler Name: | Mckesson (Sunmark) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100709 |
Package Information of Motion sickness
| Package NDC: | 49348-363-67 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (49348-363-67) > 8 TABLET in 1 BLISTER PACK |
NDC Information of Motion sickness
| NDC Code | 49348-363-67 |
| Proprietary Name | Motion sickness |
| Package Description | 1 BLISTER PACK in 1 CARTON (49348-363-67) > 8 TABLET in 1 BLISTER PACK |
| Product NDC | 49348-363 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Meclizine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100709 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mckesson (Sunmark) |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
