METOPROLOL SUCCINATE

Product NDC
0527-2603
11-digit product format
005272603
Labeler code
0527
Product ID
0527-2603_1854fb73-0c58-4edd-8b19-8e7d07b1b0d2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol succinate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Lannett Company, Inc.
Application
NDA019962
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2018-01-01
Marketing end
0000-00-00
Substance
METOPROLOL SUCCINATE
Active strength
200 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#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0527-2603-37EA - Each0527-2603a1e5828d-2de3-46f3-9da8-8b567769f0a912018-01-12
0527-2603-43EA - Each0527-2603212f9835-f31c-4136-b659-9b1a55e5558212018-01-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0527-2603METOPROLOL SUCCINATE TABLET, EXTENDED RELEASE [LANNETT COMPANY, INC.]2Legacy NDC20200429_e59f7bb8-5ed7-4c8a-969e-c9905cefcdbb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0527-2603-3700527260337100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2603-37) 2018-01-010000-00-00NoNoCurrent
0527-2603-43005272603431000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2603-43) 2018-01-010000-00-00NoNoCurrent