Amiloride Hydrochloride

Product NDC

42291-122

11-digit product format

422910122

Labeler code

42291

Product ID

42291-122_62d4c259-7915-719c-e053-2a91aa0a35de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amiloride Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA079133

Marketing category

ANDA

Marketing start

2012-03-28

Marketing end

0000-00-00

Substance

AMILORIDE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record