Verapamil Hydrochloride

Product NDC
63629-4353
11-digit product format
636294353
Labeler code
63629
Product ID
63629-4353_9a4567b7-65d9-4017-9075-4378e4b8de4c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
verapamil hydrochloride
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA019614
Marketing category
NDA
Marketing start
1990-05-29
Marketing end
0000-00-00
Substance
VERAPAMIL HYDROCHLORIDE
Active strength
360 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
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63629-4353-12020-10-12C16284748780-19855d018-d7ea-cd31-e053-dbdaa90ab51a62715866-21f7-4fb1-864f-12cb00d7f87f
63629-4353-12019-11-27C16284748780-19855d018-d7ea-cd31-e053-dbdaa90ab51a62715866-21f7-4fb1-864f-12cb00d7f87f