VENLAFAXINE HYDROCHLORIDE

Orange BookUNIISPLATC N06AX16

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

Identification

ManufacturerAlembic Pharmaceuticals Limited

CountryUS (United States)

ATC codeN06AX16

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
4670879230
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-30)
ndc11
4670879231
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-31)
ndc11
4670879271
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-71)
ndc11
4670879290
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-90)
ndc11
4670879291
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-91)

Annotations

UNII (FDA Substance ID)

7D7RX5A8MO

VENLAFAXINE HYDROCHLORIDE

RxCUI 235988

Orange Book

A217767

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": "46708-792_e3e238db-4388-49bb-aa67-6d73adbb2280",
  "productndc": "46708-792",
  "dosage_form": "CAPSULE, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "217767",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 37.5MG BASE",
        "product_no": "001",
        "approval_date": "Jun 6, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG BASE",
        "product_no": "002",
        "approval_date": "Jun 6, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 150MG BASE",
        "product_no": "003",
        "approval_date": "Jun 6, 2024"
      }
    ],
    "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": "ANDA217767",
  "marketing_category": "ANDA",
  "nonproprietary_name": "VENLAFAXINE HYDROCHLORIDE",
  "start_marketing_date": "20240610",
  "active_numerator_strength": "37.5"
}

Related drugs

Other records sharing ATC code N06AX16.

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