Metoprolol Tartrate

Product NDC
51655-536
11-digit product format
516550536
Labeler code
51655
Product ID
51655-536_1eed2ae0-5b11-49ba-abe3-9835516738f7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartrate
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
ANDA074644
Marketing category
ANDA
Marketing start
2014-09-19
Marketing end
0000-00-00
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
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
51655-536METOPROLOL TARTRATE TABLET [NORTHWIND PHARMACEUTICALS, LLC]2Legacy NDC20150401_c5d7f565-6cbe-4306-b3dd-a93ab3eac094.zip