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Fosinopril Sodium and Hydrochlorothiazide - Fosinopril Sodium and Hydrochlorothiazide

Navigation: NDC > Supplier starting with: E > EON LABS, INC.
Field Value
NDC Code: 0185-0342
Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Suffix:
Non-Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Dosage Form: TABLET
Method: ORAL
Original Marketing Date: 28-09-2005
Category Name: ANDA
Application Number: ANDA076961
Labeler: EON LABS, INC.
Substance Name: FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Active Numerator Strength: 20; 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: