venlafaxine hydrochloride

Orange BookUNIISPLATC N06AX16

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

Identification

ManufacturerDr.Reddy's Laboratories Ltd.

CountryUS (United States)

ATC codeN06AX16

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
5511145501
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-01)
ndc11
5511145505
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-05)
ndc11
5511145530
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-30)
ndc11
5511145560
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-60)
ndc11
5511145578
10 BLISTER PACK in 1 CARTON (55111-455-78) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (55111-455-79)
ndc11
5511145590
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-90)

Annotations

UNII (FDA Substance ID)

7D7RX5A8MO

VENLAFAXINE HYDROCHLORIDE

RxCUI 235988

Orange Book

A078421

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": "55111-455_a0b75dbc-2382-70bc-7bd9-c6ef3ee4ed3e",
  "productndc": "55111-455",
  "dosage_form": "CAPSULE, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "078421",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 37.5MG BASE",
        "product_no": "001",
        "approval_date": "May 6, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG BASE",
        "product_no": "002",
        "approval_date": "May 6, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 150MG BASE",
        "product_no": "003",
        "approval_date": "May 6, 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": "ANDA078421",
  "marketing_category": "ANDA",
  "nonproprietary_name": "venlafaxine hydrochloride",
  "start_marketing_date": "20110601",
  "active_numerator_strength": "150"
}

Related drugs

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