PHENDIMETRAZINE TARTRATE
Phendimetrazine Tartrate Tablets USP, 35 mg CIII Rx only
Approved
Approval ID
cc9a0cd2-6fb9-47ab-8e39-146d2fa361c2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 2, 2019
Manufacturers
FDA
Virtus Pharmaceuticals, LLC
DUNS: 079659493
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
PHENDIMETRAZINE TARTRATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69543-410
Application NumberANDA085588
Product Classification
M
Marketing Category
C73584
G
Generic Name
PHENDIMETRAZINE TARTRATE
Product Specifications
Route of AdministrationORAL
Effective DateJuly 10, 2018
FDA Product Classification
INGREDIENTS (8)
PHENDIMETRAZINE TARTRATEActive
Quantity: 35 mg in 1 1
Code: 6985IP0T80
Classification: ACTIB
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
POVIDONE, UNSPECIFIEDInactive
Code: FZ989GH94E
Classification: IACT
FD&C YELLOW NO. 5Inactive
Code: I753WB2F1M
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
SUCROSEInactive
Code: C151H8M554
Classification: IACT