NDC 21695-046

Effexor XR Extended-Release

Venlafaxine Hydrochloride

Effexor XR Extended-Release is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Venlafaxine Hydrochloride.

Product ID21695-046_8a2302ca-5c25-4d2d-9ffe-320080934aab
NDC21695-046
Product TypeHuman Prescription Drug
Proprietary NameEffexor XR Extended-Release
Generic NameVenlafaxine Hydrochloride
Dosage FormCapsule, Extended Release
Route of AdministrationORAL
Marketing Start Date1997-11-01
Marketing CategoryNDA / NDA
Application NumberNDA020699
Labeler NameRebel Distributors Corp
Substance NameVENLAFAXINE HYDROCHLORIDE
Active Ingredient Strength75 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 21695-046-90

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-046-90)
Marketing Start Date1997-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 21695-046-30 [21695004630]

Effexor XR Extended-Release CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-11-01
Inactivation Date2019-09-24

NDC 21695-046-15 [21695004615]

Effexor XR Extended-Release CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-11-01
Inactivation Date2019-09-24

NDC 21695-046-90 [21695004690]

Effexor XR Extended-Release CAPSULE, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020699
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-11-01
Inactivation Date2019-09-24

Drug Details

Active Ingredients

IngredientStrength
VENLAFAXINE HYDROCHLORIDE75 mg/1

OpenFDA Data

SPL SET ID:8a2302ca-5c25-4d2d-9ffe-320080934aab
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 729929
  • 729932
  • 729931
  • 313583
  • 313581
  • 313585
  • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    21695-047Effexor XR Extended-ReleaseEffexor XR Extended-Release
    21695-046Effexor XR Extended-ReleaseEffexor XR Extended-Release
    21695-045Effexor XR Extended-ReleaseEffexor XR Extended-Release
    67544-189Effexor XR Extended-ReleaseEffexor XR Extended-Release
    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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