Metoprolol Tartrate

Product NDC
68788-8211
11-digit product format
687888211
Labeler code
68788
Product ID
68788-8211_c4e02190-9362-4dd8-bbe3-2fcf0c2e8ecf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA200981
Marketing category
ANDA
Marketing start
2022-06-07
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
Rxcui866514

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
68788-8211-1Metoprolol Tartrate100 in 1 BOTTLETABLET, FILM COATED1003
68788-8211-3Metoprolol Tartrate30 in 1 BOTTLETABLET, FILM COATED303
68788-8211-6Metoprolol Tartrate60 in 1 BOTTLETABLET, FILM COATED603
68788-8211-9Metoprolol Tartrate90 in 1 BOTTLETABLET, FILM COATED903

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-8211-1EA - Each68788-82119a88f1ea-a0f5-4ee3-989e-8af3be3d0d4612022-07-06
68788-8211-3EA - Each68788-82113fb2a912-9b62-472a-9899-aa4d6dd2b03612022-07-06
68788-8211-6EA - Each68788-821191e8e4e6-356c-4181-b47b-9cc6051a081112022-07-06
68788-8211-9EA - Each68788-821177e6e303-a682-41d9-ac39-bb3e96746dd512022-07-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-8211METOPROLOL TARTRATE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]2Current NDC, Legacy NDC, 4 package rows20240117_5fd16fbd-be05-49aa-86a9-0f775c1b5a37.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
866514metoprolol tartrate 50 MG Oral TabletPSN5fd16fbd-be05-49aa-86a9-0f775c1b5a373
866514metoprolol tartrate 50 MG Oral TabletSCD5fd16fbd-be05-49aa-86a9-0f775c1b5a373

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-8211-168788821101100 TABLET, FILM COATED in 1 BOTTLE (68788-8211-1) 2022-06-070000-00-00NoNoCurrent
68788-8211-36878882110330 TABLET, FILM COATED in 1 BOTTLE (68788-8211-3) 2022-06-070000-00-00NoNoCurrent
68788-8211-66878882110660 TABLET, FILM COATED in 1 BOTTLE (68788-8211-6) 2022-06-070000-00-00NoNoCurrent
68788-8211-96878882110990 TABLET, FILM COATED in 1 BOTTLE (68788-8211-9) 2022-06-070000-00-00NoNoCurrent