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Last Updated: April 19, 2024

Details for New Drug Application (NDA): 020186


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NDA 020186 describes ZIAC, which is a drug marketed by Teva Branded Pharm and is included in one NDA. It is available from three suppliers. Additional details are available on the ZIAC profile page.

The generic ingredient in ZIAC is bisoprolol fumarate; hydrochlorothiazide. There are twelve drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the bisoprolol fumarate; hydrochlorothiazide profile page.
Summary for 020186
Tradename:ZIAC
Applicant:Teva Branded Pharm
Ingredient:bisoprolol fumarate; hydrochlorothiazide
Patents:0
Pharmacology for NDA: 020186
Mechanism of ActionAdrenergic beta-Antagonists
Physiological EffectIncreased Diuresis
Suppliers and Packaging for NDA: 020186
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
ZIAC bisoprolol fumarate; hydrochlorothiazide TABLET;ORAL 020186 NDA AUTHORIZED GENERIC Teva Pharmaceuticals USA, Inc. 0093-3241 0093-3241-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-3241-01)
ZIAC bisoprolol fumarate; hydrochlorothiazide TABLET;ORAL 020186 NDA AUTHORIZED GENERIC Teva Pharmaceuticals USA, Inc. 0093-3242 0093-3242-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-3242-01)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength5MG;6.25MG
Approval Date:Mar 26, 1993TE:ABRLD:Yes

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength10MG;6.25MG
Approval Date:Mar 26, 1993TE:ABRLD:Yes

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength2.5MG;6.25MG
Approval Date:Mar 26, 1993TE:ABRLD:Yes

Expired US Patents for NDA 020186

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