Rx Act all day allergy relief - Cetirizine Hydrochloride
Navigation: NDC > Supplier starting with: H > H E B| Field | Value |
|---|---|
| NDC Code: | 37808-458 |
| Proprietary Name: | Rx Act all day allergy relief |
| Suffix: | |
| Non-Proprietary Name: | Cetirizine Hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 31-01-2008 |
| Category Name: | ANDA |
| Application Number: | ANDA078336 |
| Labeler: | H E B |
| Substance Name: | CETIRIZINE HYDROCHLORIDE |
| Active Numerator Strength: | 10 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |