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Meclizine Hydrochloride
Meclizine Hydrochloride - 0781-1375-01 - (Meclizine Hydrochloride)
Drug Information of Meclizine Hydrochloride
| Product NDC: | 0781-1375 |
| Proprietary Name: | Meclizine Hydrochloride |
| 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) |
Labeler Information of Meclizine Hydrochloride
| Product NDC: | 0781-1375 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19890522 |
Package Information of Meclizine Hydrochloride
| Package NDC: | 0781-1375-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0781-1375-01) |
NDC Information of Meclizine Hydrochloride
| NDC Code | 0781-1375-01 |
| Proprietary Name | Meclizine Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (0781-1375-01) |
| Product NDC | 0781-1375 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Meclizine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19890522 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sandoz Inc |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
