Cetirizine Hydrochloride - cetirizine hydrochloride
Navigation: NDC > Supplier starting with: M > MYLAN PHARMACEUTICALS INC.| Field | Value |
|---|---|
| NDC Code: | 0378-3635 |
| Proprietary Name: | Cetirizine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | cetirizine hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 14-12-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA076677 |
| Labeler: | MYLAN PHARMACEUTICALS INC. |
| Substance Name: | CETIRIZINE HYDROCHLORIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |