| NDC Code: |
47335-175 |
| Proprietary Name: |
Levocetirizine Dihydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
Levocetirizine Dihydrochloride |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
05-02-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA090362 |
| Labeler: |
SUN PHARMA GLOBAL FZE |
| Substance Name: |
LEVOCETIRIZINE DIHYDROCHLORIDE |
| Active Numerator Strength: |
5 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule: |
|
