Losartan Potassium

Product NDC

68645-578

11-digit product format

686450578

Labeler code

68645

Product ID

68645-578_911c89d4-7b3c-4357-b7bc-0c9d9db9cd29

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

ANDA203835

Marketing category

ANDA

Marketing start

2015-08-19

Marketing end

2020-03-31

Substance

LOSARTAN POTASSIUM

Active strength

50 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record