VENLAFAXINE HYDROCHLORIDE

Orange BookUNIISPLATC N06AX16

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBluePoint Laboratories

CountryUS (United States)

ATC codeN06AX16

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6800149604
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-496-04)

Annotations

UNII (FDA Substance ID)

7D7RX5A8MO

VENLAFAXINE HYDROCHLORIDE

RxCUI 235988

Orange Book

A214419

ABABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7D7RX5A8MO",
    "rxcui": "235988",
    "inchikey": "QYRYFNHXARDNFZ-UHFFFAOYSA-N",
    "display_name": "VENLAFAXINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "b865c175-e75d-4cb4-ac29-dec72226302c": {
      "match": "brand_token",
      "title": "VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTHSTAR RXLLC]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "68001-496_2b5c3dc6-9055-abe9-e063-6294a90af76e",
  "productndc": "68001-496",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "214419",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 37.5MG BASE",
        "product_no": "001",
        "approval_date": "Oct 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG BASE",
        "product_no": "002",
        "approval_date": "Oct 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 150MG BASE",
        "product_no": "003",
        "approval_date": "Oct 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 225MG BASE",
        "product_no": "004",
        "approval_date": "Oct 21, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "VENLAFAXINE HYDROCHLORIDE",
  "proprietary_name": "VENLAFAXINE HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA214419",
  "marketing_category": "ANDA",
  "nonproprietary_name": "venlafaxine",
  "start_marketing_date": "20210430",
  "active_numerator_strength": "37.5"
}

Related drugs

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