Home
>
National Drug Code (NDC)
>
cetirizine hydrochloride
cetirizine hydrochloride - 57664-181-31 - (cetirizine hydrochloride)
Drug Information of cetirizine hydrochloride
| Product NDC: | 57664-181 |
| Proprietary Name: | cetirizine hydrochloride |
| Non Proprietary Name: | cetirizine hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; cetirizine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of cetirizine hydrochloride
| Product NDC: | 57664-181 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090191 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091116 |
Package Information of cetirizine hydrochloride
| Package NDC: | 57664-181-31 |
| Package Description: | 120 mL in 1 BOTTLE, GLASS (57664-181-31) |
NDC Information of cetirizine hydrochloride
| NDC Code | 57664-181-31 |
| Proprietary Name | cetirizine hydrochloride |
| Package Description | 120 mL in 1 BOTTLE, GLASS (57664-181-31) |
| Product NDC | 57664-181 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cetirizine hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20091116 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
