SULAR

Product NDC
59630-501
11-digit product format
596300501
Labeler code
59630
Product ID
59630-501_afb5a339-f18f-4850-8041-24859b814174
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nisoldipine
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Shionogi Inc.
Application
NDA020356
Marketing category
NDA
Marketing start
1995-02-02
Marketing end
0000-00-00
Substance
NISOLDIPINE
Active strength
17 mg/1
Pharmacologic classes
Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59630-501-10EA - Each59630-501e460b216-cc90-40ac-8721-b7026320bca312012-07-24