Venlafaxine hydrochloride
Venlafaxine HCL ER 75mg Capsule
Approved
Approval ID
f89bcae0-e714-599a-e053-6294a90a2c3a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 5, 2023
Manufacturers
FDA
Advanced Rx Pharmacy of Tennessee, LLC
DUNS: 117023142
Products 1
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 Code80425-0296
Application NumberANDA200834
Product Classification
M
Marketing Category
C73584
G
Generic Name
Venlafaxine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateApril 5, 2023
FDA Product Classification
INGREDIENTS (1)
VENLAFAXINE HYDROCHLORIDEActive
Quantity: 75 mg in 1 1
Code: 7D7RX5A8MO
Classification: ACTIM