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United States · US · US:70771-1112_466a6bd5-32e1-44ef-8220-90efc2e226d9

Doxazosin

Orange BookUNIISPLATC C02CA04

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

Identification

ManufacturerZydus Lifesciences Limited
CountryUS (United States)
ATC codeC02CA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    7077111120
    1000 TABLET in 1 BOTTLE (70771-1112-0)
  • ndc11
    7077111121
    100 TABLET in 1 BOTTLE (70771-1112-1)
  • ndc11
    7077111123
    30 TABLET in 1 BOTTLE (70771-1112-3)
  • ndc11
    7077111124
    10 BLISTER PACK in 1 CARTON (70771-1112-4) / 10 TABLET in 1 BLISTER PACK (70771-1112-2)

Annotations

UNII (FDA Substance ID)
86P6PQK0MU
DOXAZOSIN MESYLATE
RxCUI 39173
Orange Book
A208719
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "86P6PQK0MU",
    "rxcui": "39173",
    "inchikey": "VJECBOKJABCYMF-UHFFFAOYSA-N",
    "display_name": "DOXAZOSIN MESYLATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "2ea9bb6b-a4f0-496a-b27b-4454167a4b70": {
      "match": "brand_token",
      "title": "DOXAZOSIN TABLET [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "21",
      "published_date": "2026-05-15"
    }
  },
  "productid": "70771-1112_466a6bd5-32e1-44ef-8220-90efc2e226d9",
  "productndc": "70771-1112",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "208719",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 1MG BASE",
        "product_no": "001",
        "approval_date": "Jul 7, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 2MG BASE",
        "product_no": "002",
        "approval_date": "Jul 7, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 4MG BASE",
        "product_no": "003",
        "approval_date": "Jul 7, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 8MG BASE",
        "product_no": "004",
        "approval_date": "Jul 7, 2017"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DOXAZOSIN MESYLATE",
  "proprietary_name": "Doxazosin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA208719",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Doxazosin",
  "start_marketing_date": "20170831",
  "active_numerator_strength": "1"
}

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