Losartan Potassium

Product NDC
68645-411
11-digit product format
686450411
Labeler code
68645
Product ID
68645-411_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
2019-09-30
Substance
LOSARTAN POTASSIUM
Active strength
100 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
68645-411-54EA - Each68645-411ddb25bcd-f259-41a6-9432-11c60a730f4512017-03-06
68645-411-70EA - Each68645-4113be8d4e3-6dcb-42d8-bc56-d72a254c2c0812013-02-13