Losartan Potassium

Product NDC
68645-577
11-digit product format
686450577
Labeler code
68645
Product ID
68645-577_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
2020-02-29
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
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68645-577-54EA - Each68645-577cde1d221-8c37-4203-83e4-1aa47a41d05612018-04-19