Home
>
National Drug Code (NDC)
>
ZYRTEC
ZYRTEC - 50580-779-25 - (Cetirizine Hydrochloride)
Drug Information of ZYRTEC
| Product NDC: | 50580-779 |
| Proprietary Name: | ZYRTEC |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZYRTEC
| Product NDC: | 50580-779 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022429 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100208 |
Package Information of ZYRTEC
| Package NDC: | 50580-779-25 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (50580-779-25) > 25 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of ZYRTEC
| NDC Code | 50580-779-25 |
| Proprietary Name | ZYRTEC |
| Package Description | 1 BOTTLE in 1 PACKAGE (50580-779-25) > 25 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 50580-779 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20100208 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
