Amiloride Hydrochloride

Product NDC

64980-151

11-digit product format

649800151

Labeler code

64980

Product ID

64980-151_80c82512-6560-137f-e053-2a91aa0a03ea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amiloride Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Rising Pharmaceuticals, Inc

Application

ANDA079133

Marketing category

ANDA

Marketing start

2009-05-01

Marketing end

2019-07-31

Substance

AMILORIDE HYDROCHLORIDE ANHYDROUS

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

0000-00-00

Current FDA listing

Historical FDA.report record