Losartan potassium

Product NDC

70518-0789

11-digit product format

705180789

Labeler code

70518

Product ID

70518-0789_8ec959ba-ff63-9369-e053-2a95a90af3ea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

losartan potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077424

Marketing category

ANDA

Marketing start

2017-10-13

Marketing end

0000-00-00

Substance

LOSARTAN POTASSIUM

Active strength

25 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