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ZYRTEC
ZYRTEC - 50580-729-75 - (Cetirizine Hydrochloride)
Drug Information of ZYRTEC
| Product NDC: | 50580-729 |
| Proprietary Name: | ZYRTEC |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZYRTEC
| Product NDC: | 50580-729 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019835 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080101 |
Package Information of ZYRTEC
| Package NDC: | 50580-729-75 |
| Package Description: | 75 TABLET, FILM COATED in 1 PACKAGE, COMBINATION (50580-729-75) |
NDC Information of ZYRTEC
| NDC Code | 50580-729-75 |
| Proprietary Name | ZYRTEC |
| Package Description | 75 TABLET, FILM COATED in 1 PACKAGE, COMBINATION (50580-729-75) |
| Product NDC | 50580-729 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080101 |
| 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 |
