| NDC Code: |
47335-330 |
| Proprietary Name: |
CHLOROTHIAZIDE SODIUM |
| Suffix: |
|
| Non-Proprietary Name: |
CHLOROTHIAZIDE SODIUM |
| Dosage Form: |
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Method: |
INTRAVENOUS |
| Original Marketing Date: |
05-08-2011 |
| Category Name: |
ANDA |
| Application Number: |
ANDA091546 |
| Labeler: |
SUN PHARMA GLOBAL FZE |
| Substance Name: |
CHLOROTHIAZIDE SODIUM |
| Active Numerator Strength: |
500 |
| Active Ingredient Unit: |
mg/18mL |
| Pharm Classes: |
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |
|
