Losartan Potassium

Product NDC
68071-1986
11-digit product format
680711986
Labeler code
68071
Product ID
68071-1986_4443a885-c2e5-070a-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan Potassium
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA090467
Marketing category
ANDA
Marketing start
2010-10-06
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-1986-32020-07-06C16284748780-19d75b9d1-1fbf-f424-e053-dadaa90a57ce4443d937-d046-0eee-e054-00144ff88e88
68071-1986-32020-01-31C16284748780-19d75b9d1-1fbf-f424-e053-dadaa90a57ce4443d937-d046-0eee-e054-00144ff88e88