Verapamil Hydrochloride

Product NDC
63629-7845
11-digit product format
636297845
Labeler code
63629
Product ID
63629-7845_3e72c0cc-9970-4047-bb04-5e9d59160797
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
verapamil hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075138
Marketing category
ANDA
Marketing start
1999-05-20
Marketing end
0000-00-00
Substance
VERAPAMIL HYDROCHLORIDE
Active strength
120 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63629-7845-16362978450130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-7845-1) 2021-12-230000-00-00NoNoCurrent
63629-7845-26362978450260 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-7845-2) 2021-12-230000-00-00NoNoCurrent
63629-7845-36362978450390 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-7845-3) 2021-12-230000-00-00NoNoCurrent