Fosinopril Sodium And Hydrochlorothiazide 69097-0973-07

Package NDC

69097-0973-07

Manufacturer: Cipla Usa Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 24, 2020
Listing Expires: December 31, 2026
Application: ANDA090228

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Active Ingredients

Ingredient	Strength
Fosinopril Sodium	20 mg/1
Hydrochlorothiazide	12.5 mg/1

Drug Class

Thiazide Diuretic [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]

Selected Package

69097-0973-07Selected

100 TABLET in 1 BOTTLE (69097-973-07)