Cetirizine Hydrochloride - Cetirizine Hydrochloride
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NDC Code: | 51660-939 |
Proprietary Name: | Cetirizine Hydrochloride |
Suffix: | |
Non-Proprietary Name: | Cetirizine Hydrochloride |
Dosage Form: | TABLET |
Method: | ORAL |
Original Marketing Date: | 27-12-2007 |
Category Name: | ANDA |
Application Number: | ANDA077498 |
Labeler: | OHM LABORATORIES INC. |
Substance Name: | CETIRIZINE HYDROCHLORIDE |
Active Numerator Strength: | 10 |
Active Ingredient Unit: | mg/1 |
Pharm Classes: | |
DEA Schedule: |