Venlafaxine Hydrochloride

Orange BookUNIISPLATC N06AX16

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

Identification

ManufacturerAurobindo Pharma Limited

CountryUS (United States)

ATC codeN06AX16

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
6586252801
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-528-01)
ndc11
6586252810
10 BLISTER PACK in 1 CARTON (65862-528-10) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
ndc11
6586252830
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-528-30)
ndc11
6586252835
3500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-528-35)
ndc11
6586252847
15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-528-47)
ndc11
6586252890
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-528-90)
ndc11
6586252899
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-528-99)

Annotations

UNII (FDA Substance ID)

7D7RX5A8MO

VENLAFAXINE HYDROCHLORIDE

RxCUI 235988

Orange Book

A200834

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": "65862-528_d3f9b554-05be-484f-b9e7-5c8e6b2de9c9",
  "productndc": "65862-528",
  "dosage_form": "CAPSULE, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "200834",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 37.5MG BASE",
        "product_no": "001",
        "approval_date": "Apr 14, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG BASE",
        "product_no": "002",
        "approval_date": "Apr 14, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 150MG BASE",
        "product_no": "003",
        "approval_date": "Apr 14, 2011"
      }
    ],
    "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": "ANDA200834",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Venlafaxine Hydrochloride",
  "start_marketing_date": "20110601",
  "active_numerator_strength": "75"
}

Related drugs

Other records sharing ATC code N06AX16.

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