Clonidine Hydrochloride

Orange BookUNIISPLATC C02AC01

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeC02AC01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133526921
30 TABLET in 1 BOTTLE (71335-2692-1)
ndc11
7133526922
60 TABLET in 1 BOTTLE (71335-2692-2)
ndc11
7133526923
100 TABLET in 1 BOTTLE (71335-2692-3)
ndc11
7133526924
90 TABLET in 1 BOTTLE (71335-2692-4)
ndc11
7133526925
120 TABLET in 1 BOTTLE (71335-2692-5)
ndc11
7133526926
14 TABLET in 1 BOTTLE (71335-2692-6)
ndc11
7133526927
15 TABLET in 1 BOTTLE (71335-2692-7)
ndc11
7133526928
20 TABLET in 1 BOTTLE (71335-2692-8)

Annotations

UNII (FDA Substance ID)

W76I6XXF06

CLONIDINE HYDROCHLORIDE

RxCUI 142432

Orange Book

A202297

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "W76I6XXF06",
    "rxcui": "142432",
    "inchikey": "ZNIFSRGNXRYGHF-UHFFFAOYSA-N",
    "display_name": "CLONIDINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "ea1527a5-4939-4ff7-a827-f88a9113a07d": {
      "match": "brand_token",
      "title": "CLONIDINE HYDROCHLORIDE TABLET [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "15",
      "published_date": "2026-05-28"
    }
  },
  "productid": "71335-2692_4082d9a5-6176-484a-ab83-d49589a6e286",
  "productndc": "71335-2692",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202297",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "0.1MG",
        "product_no": "001",
        "approval_date": "Jun 13, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "0.2MG",
        "product_no": "002",
        "approval_date": "Jun 13, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "0.3MG",
        "product_no": "003",
        "approval_date": "Jun 13, 2013"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CLONIDINE HYDROCHLORIDE",
  "proprietary_name": "Clonidine Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202297",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Clonidine Hydrochloride",
  "start_marketing_date": "20200701",
  "active_numerator_strength": ".2"
}

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