Metoprolol Tartrate

Product NDC
63629-1462
11-digit product format
636291462
Labeler code
63629
Product ID
63629-1462_34eae92c-c44e-48b6-8f69-83ac7a5aacce
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078459
Marketing category
ANDA
Marketing start
2009-03-15
Marketing end
0000-00-00
Substance
METOPROLOL TARTRATE
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-1462-1EA - Each63629-1462e532e3c2-9dd3-4709-9278-331c833502fc12012-07-24
63629-1462-2EA - Each63629-146294768865-bb51-45e1-810f-2496fa5d691f12012-07-24
63629-1462-3EA - Each63629-146268b9c0c4-6571-406e-bde3-492930acb5fd12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63629-1462-16362914620130 TABLET, FILM COATED in 1 BOTTLE (63629-1462-1) 2009-03-150000-00-00NoNoCurrent
63629-1462-263629146202100 TABLET, FILM COATED in 1 BOTTLE (63629-1462-2) 2009-03-150000-00-00NoNoCurrent
63629-1462-36362914620360 TABLET, FILM COATED in 1 BOTTLE (63629-1462-3) 2009-03-150000-00-00NoNoCurrent
63629-1462-46362914620490 TABLET, FILM COATED in 1 BOTTLE (63629-1462-4) 2009-03-150000-00-00NoNoCurrent
63629-1462-563629146205180 TABLET, FILM COATED in 1 BOTTLE (63629-1462-5) 2009-03-150000-00-00NoNoCurrent