Cetirizine Hydrochloride - Cetirizine Hydrochloride
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-343 |
| Proprietary Name: | Cetirizine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Cetirizine Hydrochloride |
| Dosage Form: | TABLET, CHEWABLE |
| Method: | ORAL |
| Original Marketing Date: | 26-09-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA090142 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | CETIRIZINE HYDROCHLORIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |