Metoprolol Tartrate

Product NDC
51655-584
11-digit product format
516550584
Labeler code
51655
Product ID
51655-584_be7dcdea-dbe5-444b-8684-a0eab99e2676
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartrate
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
ANDA074644
Marketing category
ANDA
Marketing start
2014-09-12
Marketing end
0000-00-00
Substance
METOPROLOL TARTRATE
Active strength
100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
METOPROLOL TARTRATEACTIVE INGREDIENTW5S57Y3A5LMETOPROLOL TARTRATE TABLET [NORTHWIND PHARMACEUTICALS, LLC]2
METOPROLOLACTIVE MOIETYGEB06NHM23METOPROLOL TARTRATE TABLET [NORTHWIND PHARMACEUTICALS, LLC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-584METOPROLOL TARTRATE TABLET [NORTHWIND PHARMACEUTICALS, LLC]2Legacy NDC20150407_a84d3f91-cef2-47a2-86b5-a86526f150fd.zip