NDC 0008-0837

Effexor XR

Venlafaxine Hydrochloride

Effexor XR is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The primary component is Venlafaxine Hydrochloride.

Product ID0008-0837_0a5ea9cc-56af-4474-a69e-443eed935fc8
NDC0008-0837
Product TypeHuman Prescription Drug
Proprietary NameEffexor XR
Generic NameVenlafaxine Hydrochloride
Dosage FormCapsule, Extended Release
Route of AdministrationORAL
Marketing Start Date1997-11-01
Marketing CategoryNDA / NDA
Application NumberNDA020699
Labeler NameWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Substance NameVENLAFAXINE HYDROCHLORIDE
Active Ingredient Strength38 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0008-0837-03

100 BLISTER PACK in 1 CARTON (0008-0837-03) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0008-0837-02)
Marketing Start Date1997-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0008-0837-20 [00008083720]

Effexor XR CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-11-01

NDC 0008-0837-21 [00008083721]

Effexor XR CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-11-01

NDC 0008-0837-22 [00008083722]

Effexor XR CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-11-01

NDC 0008-0837-03 [00008083703]

Effexor XR CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-11-01

NDC 0008-0837-02 [00008083702]

Effexor XR CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-09-30

Drug Details

Active Ingredients

IngredientStrength
VENLAFAXINE HYDROCHLORIDE37.5 mg/1

OpenFDA Data

SPL SET ID:53c3e7ac-1852-4d70-d2b6-4fca819acf26
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 729929
  • 729932
  • 729931
  • 313583
  • 313581
  • 313585
    • UPC Code
  • 0300080837207

    • Pharmacological Class

    • Norepinephrine Uptake Inhibitors [MoA]
    • Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "Effexor XR" or generic name "Venlafaxine Hydrochloride"

    NDCBrand NameGeneric Name
    55289-277Effexor XREffexor XR
    70518-2156Effexor XREffexor XR
    70518-2157Effexor XREffexor XR
    80425-0088Effexor XREffexor XR
    0008-0833EffexorVENLAFAXINE HYDROCHLORIDE
    0008-0836EffexorVENLAFAXINE HYDROCHLORIDE
    0008-0837EffexorVENLAFAXINE HYDROCHLORIDE
    0093-0199Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7380Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7381Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7382Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7383Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7384Venlafaxine HydrochlorideVenlafaxine Hydrochloride

    Trademark Results [Effexor]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    EFFEXOR
    EFFEXOR
    98438579 not registered Live/Pending
    Viatris Specialty LLC
    2024-03-07
    EFFEXOR
    EFFEXOR
    74229208 1787331 Live/Registered
    WYETH LLC
    1991-12-11
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