Home
>
National Drug Code (NDC)
>
Cetirizine Hydrochloride
Cetirizine Hydrochloride - 65162-003-86 - (Cetirizine)
Drug Information of Cetirizine Hydrochloride
| Product NDC: | 65162-003 |
| Proprietary Name: | Cetirizine Hydrochloride |
| Non Proprietary Name: | Cetirizine |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Cetirizine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine Hydrochloride
| Product NDC: | 65162-003 |
| Labeler Name: | Amneal Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090765 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091007 |
Package Information of Cetirizine Hydrochloride
| Package NDC: | 65162-003-86 |
| Package Description: | 1 BOTTLE in 1 CARTON (65162-003-86) > 118 mL in 1 BOTTLE |
NDC Information of Cetirizine Hydrochloride
| NDC Code | 65162-003-86 |
| Proprietary Name | Cetirizine Hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (65162-003-86) > 118 mL in 1 BOTTLE |
| Product NDC | 65162-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091007 |
| Marketing Category Name | ANDA |
| Labeler Name | Amneal Pharmaceuticals |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
