NDC 65862-308-01
Fosinopril Sodium and Hydrochlorothiazide 10 mg/1
Fosinopril Sodium and Hydrochlorothiazide · TABLET
Fosinopril Sodium and Hydrochlorothiazide is a tablet containing fosinopril sodium and hydrochlorothiazide at a strength of 10 mg/1. Manufactured by Aurobindo Pharma Limited.
Key Facts
- Brand Name
- Fosinopril Sodium and Hydrochlorothiazide
- Generic Name
- Fosinopril Sodium and Hydrochlorothiazide
- NDC Code (Package)
65862-308-01- NDC Code (Product)
65862-308- Manufacturer
- Aurobindo Pharma Limited
- Strength
- 10 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA079245
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 07/09/2009
Recall History
No Recall HistoryView Full Drug Page
Fosinopril Sodium and Hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.