Losartan Potassium

Product NDC
55700-474
11-digit product format
557000474
Labeler code
55700
Product ID
55700-474_6ea81244-0cae-44a6-9070-4e037c1a36b0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA091497
Marketing category
ANDA
Marketing start
2017-01-13
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-474-30EA - Each55700-474b5d5916c-1fd7-47db-8933-0578c9b182c012017-03-06