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Cyclivert
Cyclivert - 16477-401-01 - (CYCLIZINE HYDROCHLORIDE)
Drug Information of Cyclivert
| Product NDC: | 16477-401 |
| Proprietary Name: | Cyclivert |
| Non Proprietary Name: | CYCLIZINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 mg/25mg & nbsp; CYCLIZINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclivert
| Product NDC: | 16477-401 |
| Labeler Name: | Laser Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111101 |
Package Information of Cyclivert
| Package NDC: | 16477-401-01 |
| Package Description: | 25 mg in 1 BOTTLE (16477-401-01) |
NDC Information of Cyclivert
| NDC Code | 16477-401-01 |
| Proprietary Name | Cyclivert |
| Package Description | 25 mg in 1 BOTTLE (16477-401-01) |
| Product NDC | 16477-401 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CYCLIZINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laser Pharmaceuticals, LLC |
| Substance Name | CYCLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/25mg |
| Pharmaceutical Classes |
