Fosinopril Sodium and Hydrochlorothiazide - Fosinopril Sodium and Hydrochlorothiazide
Navigation: NDC > Supplier starting with: A > AUROBINDO PHARMA LIMITED| Field | Value |
|---|---|
| NDC Code: | 65862-308 |
| Proprietary Name: | Fosinopril Sodium and Hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | Fosinopril Sodium and Hydrochlorothiazide |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 09-07-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA079245 |
| Labeler: | AUROBINDO PHARMA LIMITED |
| Substance Name: | FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: | 10; 12.5 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |