Zyrtec - Cetirizine Hydrochloride
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Field |
Value |
NDC Code: |
50580-726 |
Proprietary Name: |
Zyrtec |
Suffix: |
|
Non-Proprietary Name: |
Cetirizine Hydrochloride |
Dosage Form: |
TABLET, FILM COATED |
Method: |
ORAL |
Original Marketing Date: |
01-10-2008 |
Category Name: |
NDA |
Application Number: |
NDA019835 |
Labeler: |
MCNEIL CONSUMER HEALTHCARE DIVISION OF MCNEIL PPC, INC. |
Substance Name: |
CETIRIZINE HYDROCHLORIDE |
Active Numerator Strength: |
10 |
Active Ingredient Unit: |
mg/1 |
Pharm Classes: |
|
DEA Schedule: |
|