Metoprolol Succinate

Product NDC
64679-736
11-digit product format
646790736
Labeler code
64679
Product ID
64679-736_4b06b8e0-8d8f-4ce3-8d45-59f91190c5f4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA090615
Marketing category
ANDA
Marketing start
2010-07-22
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64679-736METOPROLOL SUCCINATE TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT USA LLC.]9Legacy NDC20191126_c20170ea-0e24-4e82-b9cb-aebdbfcc022a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
64679-736-016467907360130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-736-01) 2010-07-220000-00-00NoNoCurrent
64679-736-0264679073602100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-736-02) 2010-07-220000-00-00NoNoCurrent
64679-736-0364679073603500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-736-03) 2010-07-220000-00-00NoNoCurrent
64679-736-056467907360510 BLISTER PACK in 1 CARTON (64679-736-05) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK10 blister pack2010-07-220000-00-00NoNoCurrent
64679-736-08646790736083000 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (64679-736-08) 2010-07-220000-00-00NoNoCurrent
64679-736-096467907360912 BOTTLE in 1 CARTON (64679-736-09) > 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE12 bottle2010-07-220000-00-00NoNoCurrent