Effexor
EFFEXOR (venlafaxine hydrochloride) capsule, extended release
Approved
Approval ID
f2f03495-12b6-457a-901f-958b9c844bfd
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 27, 2009
Manufacturers
FDA
Stat Rx USA
DUNS: 786036330
Products 3
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
venlafaxine hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-086
Application NumberNDA020699
Product Classification
M
Marketing Category
C73594
G
Generic Name
venlafaxine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2009
FDA Product Classification
INGREDIENTS (1)
venlafaxine hydrochlorideActive
Quantity: 75 mg in 1 1
Code: 7D7RX5A8MO
Classification: ACTIB
venlafaxine hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-085
Application NumberNDA020699
Product Classification
M
Marketing Category
C73594
G
Generic Name
venlafaxine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2009
FDA Product Classification
INGREDIENTS (1)
venlafaxine hydrochlorideActive
Quantity: 37.5 mg in 1 1
Code: 7D7RX5A8MO
Classification: ACTIB
venlafaxine hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-087
Application NumberNDA020699
Product Classification
M
Marketing Category
C73594
G
Generic Name
venlafaxine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2009
FDA Product Classification
INGREDIENTS (1)
venlafaxine hydrochlorideActive
Quantity: 150 mg in 1 1
Code: 7D7RX5A8MO
Classification: ACTIB