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Cetirizine
Cetirizine - 63629-3708-1 - (Cetirizine Hydrochloride)
Drug Information of Cetirizine
| Product NDC: | 63629-3708 |
| Proprietary Name: | Cetirizine |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine
| Product NDC: | 63629-3708 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078336 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080116 |
Package Information of Cetirizine
| Package NDC: | 63629-3708-1 |
| Package Description: | 30 TABLET in 1 BOTTLE (63629-3708-1) |
NDC Information of Cetirizine
| NDC Code | 63629-3708-1 |
| Proprietary Name | Cetirizine |
| Package Description | 30 TABLET in 1 BOTTLE (63629-3708-1) |
| Product NDC | 63629-3708 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080116 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
