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United States · US · US:71335-1047_cd25e2c5-25ff-46ae-80ef-b01300cd959d

Hydroxyzine Hydrochloride

SPLATC 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 · 8

  • ndc11
    7133510471
    30 TABLET, FILM COATED in 1 BOTTLE (71335-1047-1)
  • ndc11
    7133510472
    60 TABLET, FILM COATED in 1 BOTTLE (71335-1047-2)
  • ndc11
    7133510473
    20 TABLET, FILM COATED in 1 BOTTLE (71335-1047-3)
  • ndc11
    7133510474
    100 TABLET, FILM COATED in 1 BOTTLE (71335-1047-4)
  • ndc11
    7133510475
    15 TABLET, FILM COATED in 1 BOTTLE (71335-1047-5)
  • ndc11
    7133510476
    90 TABLET, FILM COATED in 1 BOTTLE (71335-1047-6)
  • ndc11
    7133510477
    19 TABLET, FILM COATED in 1 BOTTLE (71335-1047-7)
  • ndc11
    7133510478
    10 TABLET, FILM COATED in 1 BOTTLE (71335-1047-8)

Annotations

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": "71335-1047_cd25e2c5-25ff-46ae-80ef-b01300cd959d",
  "productndc": "71335-1047",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "HYDROXYZINE DIHYDROCHLORIDE",
  "proprietary_name": "Hydroxyzine Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA040602",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Hydroxyzine Hydrochloride",
  "start_marketing_date": "20150331",
  "active_numerator_strength": "25"
}

Related drugs

Other records sharing ATC code N05BB01.

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