Cetirizine Hydrochloride - Cetirizine Hydrochloride
Navigation: NDC > Supplier starting with: P > PHARMACEUTICAL ASSOCIATES, INC.| Field | Value |
|---|---|
| NDC Code: | 0121-4780 |
| Proprietary Name: | Cetirizine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Cetirizine Hydrochloride |
| Dosage Form: | SYRUP |
| Method: | ORAL |
| Original Marketing Date: | 15-09-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA090300 |
| Labeler: | PHARMACEUTICAL ASSOCIATES, INC. |
| Substance Name: | CETIRIZINE HYDROCHLORIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/5mL |
| Pharm Classes: | |
| DEA Schedule: |