Metoprolol Tartrate
Approved
Approval ID
8fd17a7c-1d95-425a-b5a9-59e812225443
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 13, 2010
Manufacturers
FDA
State of Florida DOH Central Pharmacy
DUNS: 829348114
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
METOPROLOL TARTRATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code53808-0659
Application NumberANDA076670
Product Classification
M
Marketing Category
C73584
G
Generic Name
METOPROLOL TARTRATE
Product Specifications
Route of AdministrationORAL
Effective DateAugust 13, 2010
FDA Product Classification
INGREDIENTS (10)
METOPROLOL TARTRATEActive
Quantity: 25 mg in 1 1
Code: W5S57Y3A5L
Classification: ACTIB
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
POLYETHYLENE GLYCOLInactive
Code: 3WJQ0SDW1A
Classification: IACT