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Meclizine HCl
Meclizine HCl - 0536-3990-01 - (Meclizine HCl)
Drug Information of Meclizine HCl
| Product NDC: | 0536-3990 |
| Proprietary Name: | Meclizine HCl |
| 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 Meclizine HCl
| Product NDC: | 0536-3990 |
| Labeler Name: | Rugby Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080722 |
Package Information of Meclizine HCl
| Package NDC: | 0536-3990-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0536-3990-01) |
NDC Information of Meclizine HCl
| NDC Code | 0536-3990-01 |
| Proprietary Name | Meclizine HCl |
| Package Description | 100 TABLET in 1 BOTTLE (0536-3990-01) |
| Product NDC | 0536-3990 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Meclizine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080722 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories Inc. |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
