verapamil hydrochloride

Product NDC
49999-284
11-digit product format
499990284
Labeler code
49999
Product ID
49999-284_de7cfa9e-5e5f-49bf-892b-2587b99f8df9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
verapamil hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA090700
Marketing category
ANDA
Marketing start
2011-08-05
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
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
V3888OEY5RVERAPAMIL HYDROCHLORIDE152-11-4VERAPAMIL HYDROCHLORIDE