FDA.reportPublic FDA data

Metoprolol Tartrate

Product NDC
50090-2149
11-digit product format
500902149
Labeler code
50090
Product ID
50090-2149_b988019e-ae73-4ec7-be08-e9ef6a3f96ed
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077739
Marketing category
ANDA
Marketing start
2007-09-11
Substance
METOPROLOL TARTRATE
Active strength
50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Metoprolol Tartrate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METOPROLOL TARTRATE50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiW5S57Y3A5L
Rxcui866511, 866514, 866924

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fac0d979-ed64-4395-be9a-fc0b6f8c0a4fProduct name120260122
e1a63b6e-1877-c2c1-01a3-03ea2817aa6fProduct name320251027
07ea0487-5434-6896-2497-013a7ee4afbdProduct name920250311
95ced987-af5e-4bea-8119-4e7d4558d21bProduct name220200617
47fc2fe9-7afb-4be9-989d-787aaa6ad0eaProduct name120200505
9ab5a42a-e77d-486b-bb1f-b343fe664adaProduct name120180430
310125de-e7c0-730d-d178-98b990a0334aProduct name220150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-2149-0Metoprolol Tartrate30 in 1 BOTTLETABLET, FILM COATED3028
50090-2149-1Metoprolol Tartrate60 in 1 BOTTLETABLET, FILM COATED6028
50090-2149-4Metoprolol Tartrate90 in 1 BOTTLETABLET, FILM COATED9028
50090-2149-5Metoprolol Tartrate180 in 1 BOTTLETABLET, FILM COATED18028

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-2149METOPROLOL TARTRATE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]28Current NDC, Legacy NDC, 4 package rows20241004_f4e88ecc-2d9b-4bad-97dd-77b1cbb75eb0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
866511metoprolol tartrate 100 MG Oral TabletPSNf4e88ecc-2d9b-4bad-97dd-77b1cbb75eb028
866924metoprolol tartrate 25 MG Oral TabletPSNf4e88ecc-2d9b-4bad-97dd-77b1cbb75eb028
866514metoprolol tartrate 50 MG Oral TabletPSNf4e88ecc-2d9b-4bad-97dd-77b1cbb75eb028
866511metoprolol tartrate 100 MG Oral TabletSCDf4e88ecc-2d9b-4bad-97dd-77b1cbb75eb028
866924metoprolol tartrate 25 MG Oral TabletSCDf4e88ecc-2d9b-4bad-97dd-77b1cbb75eb028
866514metoprolol tartrate 50 MG Oral TabletSCDf4e88ecc-2d9b-4bad-97dd-77b1cbb75eb028

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-2149-05009021490030 TABLET, FILM COATED in 1 BOTTLE (50090-2149-0) 2015-10-200000-00-00NoNoCurrent
50090-2149-15009021490160 TABLET, FILM COATED in 1 BOTTLE (50090-2149-1) 2015-10-200000-00-00NoNoCurrent
50090-2149-45009021490490 TABLET, FILM COATED in 1 BOTTLE (50090-2149-4) 2015-10-200000-00-00NoNoCurrent
50090-2149-550090214905180 TABLET, FILM COATED in 1 BOTTLE (50090-2149-5) 2015-10-200000-00-00NoNoCurrent