Approvals (Drugs@FDA)

VENLAFAXINE HYDROCHLORIDE

YICHANG HUMANWELL · VENLAFAXINE HYDROCHLORIDE

ANDA220619Generic (ANDA)Prescription
Open FDA's page for this record
Application number
ANDA220619
Sponsor name
YICHANG HUMANWELL
Submissions
  1. Submission type
    ORIG
    Submission number
    1
    Submission status
    AP
    Submission status date
    20261106
    Review priority
    STANDARD
    Submission class code
    UNKNOWN
Products
  1. Product number
    002
    Reference drug
    No
    Brand name
    VENLAFAXINE HYDROCHLORIDE
    Reference standard
    No
    Dosage form
    CAPSULE, EXTENDED RELEASE
    Route
    ORAL
    Marketing status
    Prescription
    Te code
    AB
    Active ingredients
    1. Name
      VENLAFAXINE HYDROCHLORIDE
      Strength
      EQ 75MG BASE
  2. Product number
    003
    Reference drug
    No
    Brand name
    VENLAFAXINE HYDROCHLORIDE
    Reference standard
    No
    Dosage form
    CAPSULE, EXTENDED RELEASE
    Route
    ORAL
    Marketing status
    Prescription
    Te code
    AB
    Active ingredients
    1. Name
      VENLAFAXINE HYDROCHLORIDE
      Strength
      EQ 150MG BASE
  3. Product number
    001
    Reference drug
    No
    Brand name
    VENLAFAXINE HYDROCHLORIDE
    Reference standard
    No
    Dosage form
    CAPSULE, EXTENDED RELEASE
    Route
    ORAL
    Marketing status
    Prescription
    Te code
    AB
    Active ingredients
    1. Name
      VENLAFAXINE HYDROCHLORIDE
      Strength
      EQ 37.5MG BASE
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.