verapamil hydrochloride

Product NDC
50090-1566
11-digit product format
500901566
Labeler code
50090
Product ID
50090-1566_49a26f30-37c8-4544-aa47-f3417f50e6eb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
verapamil hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078906
Marketing category
ANDA
Marketing start
2009-09-17
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1566-0EA - Each50090-1566f8409504-c9fa-453c-96ac-d4a75545f53012018-11-06
50090-1566-4EA - Each50090-1566a9da86ee-84fd-4eda-9c6b-99e4e618795112018-08-13