Cetirizine Hydrochloride - cetirizine hydrochloride
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NDC Code: | 55154-5399 |
Proprietary Name: | Cetirizine Hydrochloride |
Suffix: | |
Non-Proprietary Name: | cetirizine hydrochloride |
Dosage Form: | TABLET, FILM COATED |
Method: | ORAL |
Original Marketing Date: | 30-03-2012 |
Category Name: | ANDA |
Application Number: | ANDA076677 |
Labeler: | CARDINAL HEALTH |
Substance Name: | CETIRIZINE HYDROCHLORIDE |
Active Numerator Strength: | 10 |
Active Ingredient Unit: | mg/1 |
Pharm Classes: | |
DEA Schedule: |