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United States · US · US:71335-3036_52f79423-8a65-411f-b83b-e314df3811c1

Hydroxyzine Hydrochloride

Orange BookSPLATC N05BB01

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN05BB01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7133530361
    1000 TABLET, FILM COATED in 1 BOTTLE (71335-3036-1)

Annotations

Orange Book
A087871
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "ORAL",
  "spl_meta": {
    "4cd84205-6a33-db48-e063-6394a90a9182": {
      "match": "brand_token",
      "title": "HYDROXYZINE HYDROCHLORIDE TABLET [NUCARE PHARMACEUTICALS, INC.]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-3036_52f79423-8a65-411f-b83b-e314df3811c1",
  "productndc": "71335-3036",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "087871",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Dec 20, 1982"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Dec 20, 1982"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "003",
        "approval_date": "Dec 20, 1982"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "HYDROXYZINE DIHYDROCHLORIDE",
  "proprietary_name": "Hydroxyzine Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA087871",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Hydroxyzine Hydrochloride",
  "start_marketing_date": "20211007",
  "active_numerator_strength": "50"
}

Related drugs

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