METOPROLOL TARTRATE

Product NDC
68788-8886
11-digit product format
687888886
Labeler code
68788
Product ID
68788-8886_4c6c75c5-9c80-44e1-bd16-b97509c9f542
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METOPROLOL TARTRATE
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA200981
Marketing category
ANDA
Marketing start
2025-06-06
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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
W5S57Y3A5LMETOPROLOL TARTRATE56392-17-7METOPROLOL TARTRATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68788-8886-168788888601100 TABLET in 1 BOTTLE (68788-8886-1) 100 tablet2025-06-06NoNoHistorical
68788-8886-36878888860330 TABLET in 1 BOTTLE (68788-8886-3) 30 tablet2025-06-06NoNoHistorical
68788-8886-66878888860660 TABLET in 1 BOTTLE (68788-8886-6) 60 tablet2025-06-06NoNoHistorical
68788-8886-96878888860990 TABLET in 1 BOTTLE (68788-8886-9) 90 tablet2025-06-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
METOPROLOL TARTRATEPreferred Pharmaceuticals Inc.2025-06-06HUMAN PRESCRIPTION DRUG LABEL1