Valsartan

Product NDC
0591-2167
11-digit product format
005912167
Labeler code
0591
Product ID
0591-2167_70122f99-a4e4-4c32-8c5c-d843df4a974e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
valsartan
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Actavis Pharma, Inc.
Application
ANDA090642
Marketing category
ANDA
Marketing start
2015-01-05
Marketing end
2019-10-31
Substance
VALSARTAN
Active strength
40 mg/1
Pharmacologic classes
Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0591-2167-19EA - Each0591-21675ce48fb9-449c-4e77-bd66-0efab86478a012015-02-02
0591-2167-30EA - Each0591-21675377c591-2e29-4a28-bf11-a5a967d0688312015-02-02