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Medtronic
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Generated: October 19, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 073209

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NDA 073209 describes AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Mylan, Barr, Watson Labs, Sandoz, and Teva, and is included in five NDAs. It is available from five suppliers. Additional details are available on the AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE profile page.

The generic ingredient in AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is amiloride hydrochloride; hydrochlorothiazide. There are five drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the amiloride hydrochloride; hydrochlorothiazide profile page.

Summary for NDA: 073209

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Formulation / Manufacturing:see details

Pharmacology for NDA: 073209

Suppliers and Packaging for NDA: 073209

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
amiloride hydrochloride; hydrochlorothiazide
TABLET;ORAL 073209 ANDA Mylan Pharmaceuticals Inc. 0378-0577 0378-0577-01 100 TABLET in 1 BOTTLE, PLASTIC (0378-0577-01)
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
amiloride hydrochloride; hydrochlorothiazide
TABLET;ORAL 073209 ANDA Mylan Pharmaceuticals Inc. 0378-0577 0378-0577-05 500 TABLET in 1 BOTTLE, PLASTIC (0378-0577-05)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrengthEQ 5MG ANHYDROUS;50MG
Approval Date:Oct 31, 1991TE:ABRLD:No


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