Losartan Potassium

Product NDC
16571-502
11-digit product format
165710502
Labeler code
16571
Product ID
16571-502_a1c2686b-bbf3-4afc-aeb5-84a2f64341e3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
losartan potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Rising Pharmaceuticals, Inc
Application
ANDA091497
Marketing category
ANDA
Marketing start
2014-07-30
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
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16571-502-11EA - Each16571-5020b5a6a9e-b4cc-4077-9286-0c04adaf5fae12012-07-24