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United States · US · US:72241-076_14b38374-7287-47dd-8ef9-e88bd5b23a26

Venlafaxine

Orange BookUNIISPLATC N06AX16

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerModavar Pharmaceuticals LLC
CountryUS (United States)
ATC codeN06AX16
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    7224107604
    90 TABLET, COATED in 1 BOTTLE (72241-076-04)
  • ndc11
    7224107611
    1000 TABLET, COATED in 1 BOTTLE (72241-076-11)
  • ndc11
    7224107622
    30 TABLET, COATED in 1 BOTTLE (72241-076-22)

Annotations

UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A211323
ABABAB
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": "72241-076_14b38374-7287-47dd-8ef9-e88bd5b23a26",
  "productndc": "72241-076",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "211323",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG BASE",
        "product_no": "001",
        "approval_date": "Aug 29, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 150MG BASE",
        "product_no": "002",
        "approval_date": "Aug 29, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 225MG BASE",
        "product_no": "003",
        "approval_date": "Aug 29, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "VENLAFAXINE HYDROCHLORIDE",
  "proprietary_name": "Venlafaxine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA211323",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Venlafaxine",
  "start_marketing_date": "20180105",
  "active_numerator_strength": "150"
}

Related drugs

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