Fexofenadine HCl and Pseudoephedrine HCl - Fexofenadine HCl and Pseudoephedrine HCl
Navigation: NDC > Supplier starting with: D > DR.REDDY'S LABORATORIES LIMITED| Field | Value |
|---|---|
| NDC Code: | 55111-572 |
| Proprietary Name: | Fexofenadine HCl and Pseudoephedrine HCl |
| Suffix: | |
| Non-Proprietary Name: | Fexofenadine HCl and Pseudoephedrine HCl |
| Dosage Form: | TABLET, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 28-01-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA079043 |
| Labeler: | DR.REDDY'S LABORATORIES LIMITED |
| Substance Name: | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Numerator Strength: | 180; 240 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
| DEA Schedule: |