Amiloride Hydrochloride

Product NDC

50268-071

11-digit product format

502680071

Labeler code

50268

Product ID

50268-071_64c9f8c6-b96f-7208-e053-2a91aa0ab6fc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amiloride Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA079133

Marketing category

ANDA

Marketing start

2013-01-28

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