Losartan Potassium

Product NDC

42708-035

11-digit product format

427080035

Labeler code

42708

Product ID

42708-035_85fa8ac7-243d-4336-8c2e-29fe6a02d18f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

QPharma Inc

Application

ANDA076958

Marketing category

ANDA

Marketing start

2010-04-06

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record