Valsartan

Product NDC
51655-751
11-digit product format
516550751
Labeler code
51655
Product ID
51655-751_3058d174-bff7-49db-8ca1-fa2d61898b9e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Valsartan
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA077492
Marketing category
ANDA
Marketing start
2015-01-07
Marketing end
0000-00-00
Substance
VALSARTAN
Active strength
160 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
51655-751-522026-01-02C16284748780-19d75b9d0-f619-f424-e053-dadaa90a57ce8841770a-ab65-4907-b036-e2eaca982411
51655-751-522020-01-31C16284748780-19d75b9d0-f619-f424-e053-dadaa90a57ce8841770a-ab65-4907-b036-e2eaca982411

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-751VALSARTAN TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]1Legacy NDC20150428_8841770a-ab65-4907-b036-e2eaca982411.zip