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ALLEROFF
ALLEROFF - 16853-1261-2 - (Cetirizine Hydrochloride)
Drug Information of ALLEROFF
| Product NDC: | 16853-1261 |
| Proprietary Name: | ALLEROFF |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 1 mg/1 & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALLEROFF
| Product NDC: | 16853-1261 |
| Labeler Name: | Corporacion Infarmasa |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022155 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100115 |
Package Information of ALLEROFF
| Package NDC: | 16853-1261-2 |
| Package Description: | 2 SYRUP in 1 PACKAGE, COMBINATION (16853-1261-2) |
NDC Information of ALLEROFF
| NDC Code | 16853-1261-2 |
| Proprietary Name | ALLEROFF |
| Package Description | 2 SYRUP in 1 PACKAGE, COMBINATION (16853-1261-2) |
| Product NDC | 16853-1261 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20100115 |
| Marketing Category Name | NDA |
| Labeler Name | Corporacion Infarmasa |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
