Cetirizine Hydrochloride - Cetirizine Hydrochloride
Navigation: NDC > Supplier starting with: B > BRECKENRIDGE PHARMACEUTICAL, INC.| Field | Value |
|---|---|
| NDC Code: | 51991-837 |
| Proprietary Name: | Cetirizine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Cetirizine Hydrochloride |
| Dosage Form: | SOLUTION |
| Method: | ORAL |
| Original Marketing Date: | 03-12-2013 |
| Category Name: | ANDA |
| Application Number: | ANDA078488 |
| Labeler: | BRECKENRIDGE PHARMACEUTICAL, INC. |
| Substance Name: | CETIRIZINE HYDROCHLORIDE |
| Active Numerator Strength: | 1 |
| Active Ingredient Unit: | mg/mL |
| Pharm Classes: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule: |