Verapamil Hydrochloride

Product NDC
51079-869
11-digit product format
510790869
Labeler code
51079
Product ID
51079-869_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
1996-04-15
Marketing end
0000-00-00
Substance
VERAPAMIL HYDROCHLORIDE
Active strength
240 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
51079-869-01EA - Each51079-869765aa9b6-982f-498e-97bd-2b46558e103312012-07-24
51079-869-20EA - Each51079-869089ede3e-d673-4803-90c1-545580caed6012012-07-24
51079-869-30EA - Each51079-86916453dbe-e69f-49e4-8bc0-c63d08b154d112012-07-24
51079-869-56EA - Each51079-86973634cdc-e277-4e16-b6f8-2bef1d4414c212012-07-24