Verapamil Hydrochloride

Product NDC
51079-899
11-digit product format
510790899
Labeler code
51079
Product ID
51079-899_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
1998-11-15
Marketing end
0000-00-00
Substance
VERAPAMIL HYDROCHLORIDE
Active strength
180 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
51079-899-01EA - Each51079-89930650cdd-ec04-4902-aa29-30544faa19cc12012-07-24
51079-899-20EA - Each51079-89958804258-1422-46d6-b5e1-ed5207b9c31d12012-07-24
51079-899-30EA - Each51079-89971a389ae-02e7-4c03-b702-f10daff9d5fd12012-07-24
51079-899-56EA - Each51079-89950acab6e-f9a7-48f6-8d02-f43e98c7290912012-07-24