Losartan Potassium

Product NDC

68645-409

11-digit product format

686450409

Labeler code

68645

Product ID

68645-409_158d10b1-a1f5-4725-bb56-9e6dadaae1dd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

ANDA076958

Marketing category

ANDA

Marketing start

2010-04-06

Marketing end

2019-11-30

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