Losartan potassium

Product NDC

70518-0419

11-digit product format

705180419

Labeler code

70518

Product ID

70518-0419_84f6a71f-5faa-cdb0-e053-2a91aa0a6209

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

2017-04-11

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