Hydroxyzine Hydrochloride - hydroxyzine hydrochloride
Navigation: NDC > Supplier starting with: Q > QUALITEST PHARMACEUTICALS| Field | Value |
|---|---|
| NDC Code: | 0603-3969 |
| Proprietary Name: | Hydroxyzine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | hydroxyzine hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 27-05-2005 |
| Category Name: | ANDA |
| Application Number: | ANDA040580 |
| Labeler: | QUALITEST PHARMACEUTICALS |
| Substance Name: | HYDROXYZINE HYDROCHLORIDE |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
| DEA Schedule: |