Verapamil Hydrochloride

Product NDC
51079-894
11-digit product format
510790894
Labeler code
51079
Product ID
51079-894_7d8f163b-f290-42cc-e053-2991aa0aef2f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
verapamil hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA074587
Marketing category
ANDA
Marketing start
1998-04-17
Marketing end
0000-00-00
Substance
VERAPAMIL HYDROCHLORIDE
Active strength
120 mg/1
Pharmacologic classes
P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
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
51079-894-01EA - Each51079-894033d3e15-7a7c-40d5-86d7-9098373a444712012-07-24
51079-894-20EA - Each51079-894858237c8-e653-457f-bad2-256a3e1339fa12012-07-24