Hydroxyzine Hydrochloride

SPLATC N05BB01

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

Identification

ManufacturerPD-Rx Pharmaceuticals, Inc.

CountryUS (United States)

ATC codeN05BB01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
4306351806
6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-06)
ndc11
4306351812
12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-12)
ndc11
4306351820
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-20)
ndc11
4306351828
28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-28)
ndc11
4306351830
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-30)
ndc11
4306351840
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-40)
ndc11
4306351860
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-60)
ndc11
4306351890
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-90)

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": "43063-518_4138e4f8-23cf-c563-e063-6294a90ad9bb",
  "productndc": "43063-518",
  "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": "ANDA040787",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Hydroxyzine Hydrochloride",
  "start_marketing_date": "20120724",
  "active_numerator_strength": "25"
}

Related drugs

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