Cetirizine Hydrochloride - Cetirizine Hydrochloride
Navigation: NDC > Supplier starting with: P > PACK PHARMACEUTICALS LLC| Field | Value |
|---|---|
| NDC Code: | 16571-402 |
| Proprietary Name: | Cetirizine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Cetirizine Hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-10-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA077829 |
| Labeler: | PACK PHARMACEUTICALS LLC |
| Substance Name: | CETIRIZINE HYDROCHLORIDE |
| Active Numerator Strength: | 10 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |