Losartan Potassium

Product NDC
0904-6389
11-digit product format
009046389
Labeler code
0904
Product ID
0904-6389_7a0e4c06-409c-47b4-ae32-88eaf64964ed
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan Potassium
Dosage form
TABLET
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA090467
Marketing category
ANDA
Marketing start
2010-10-06
Marketing end
0000-00-00
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6389-61EA - Each0904-6389e97f1332-ee81-4c68-a6c3-a72ee63c7f3f12014-10-03