Fosinopril Sodium - Fosinopril Sodium
Navigation: NDC > Supplier starting with: T > TEVA PHARMACEUTICALS USA INC| Field | Value |
|---|---|
| NDC Code: | 0093-7222 |
| Proprietary Name: | Fosinopril Sodium |
| Suffix: | |
| Non-Proprietary Name: | Fosinopril Sodium |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-12-2003 |
| Category Name: | ANDA |
| Application Number: | ANDA076139 |
| Labeler: | TEVA PHARMACEUTICALS USA INC |
| Substance Name: | FOSINOPRIL SODIUM |
| Active Numerator Strength: | 10 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
| DEA Schedule: |