Hydrochlorothiazide - Hydrochlorothiazide
Navigation: NDC > Supplier starting with: G > GREENSTONE LLC| Field | Value |
|---|---|
| NDC Code: | 59762-1737 |
| Proprietary Name: | Hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | Hydrochlorothiazide |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 20-07-2007 |
| End of Marketing: | 30-06-2014 |
| Category Name: | ANDA |
| Application Number: | ANDA040780 |
| Labeler: | GREENSTONE LLC |
| Substance Name: | HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |