venlafaxine

Orange BookUNIISPLATC N06AX16

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AX16

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
7133511041
60 TABLET in 1 BOTTLE (71335-1104-1)
ndc11
7133511042
30 TABLET in 1 BOTTLE (71335-1104-2)
ndc11
7133511043
90 TABLET in 1 BOTTLE (71335-1104-3)
ndc11
7133511044
28 TABLET in 1 BOTTLE (71335-1104-4)
ndc11
7133511045
120 TABLET in 1 BOTTLE (71335-1104-5)
ndc11
7133511046
100 TABLET in 1 BOTTLE (71335-1104-6)

Annotations

UNII (FDA Substance ID)

7D7RX5A8MO

VENLAFAXINE HYDROCHLORIDE

RxCUI 235988

Orange Book

A090555

ABABABABAB

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": "71335-1104_6feb7962-b69c-40d9-a853-f2ea11ae333f",
  "productndc": "71335-1104",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "090555",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "001",
        "approval_date": "Apr 7, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 37.5MG BASE",
        "product_no": "002",
        "approval_date": "Apr 7, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "003",
        "approval_date": "Apr 7, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG BASE",
        "product_no": "004",
        "approval_date": "Apr 7, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 100MG BASE",
        "product_no": "005",
        "approval_date": "Apr 7, 2010"
      }
    ],
    "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": "ANDA090555",
  "marketing_category": "ANDA",
  "nonproprietary_name": "venlafaxine hydrochloride",
  "start_marketing_date": "20100407",
  "active_numerator_strength": "75"
}

Related drugs

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