Metoprolol Succinate ER

Product NDC
63629-4387
11-digit product format
636294387
Labeler code
63629
Product ID
63629-4387_6fe8996f-e4e0-401d-bed8-3ed31ad346f2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077298
Marketing category
ANDA
Marketing start
2010-04-15
Marketing end
0000-00-00
Substance
METOPROLOL SUCCINATE
Active strength
100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63629-4387-16362943870130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4387-1) 2010-12-010000-00-00NoNoCurrent
63629-4387-26362943870290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4387-2) 2010-12-010000-00-00NoNoCurrent
63629-4387-363629438703120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4387-3) 2010-12-010000-00-00NoNoCurrent
63629-4387-46362943870420 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4387-4) 2010-12-010000-00-00NoNoCurrent
63629-4387-563629438705100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4387-5) 2010-12-010000-00-00NoNoCurrent
63629-4387-66362943870660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4387-6) 2010-12-010000-00-00NoNoCurrent