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United States · US · US:72789-216_3caab728-dec4-fe78-e063-6294a90a17ec
Hydroxyzine Hydrochloride
Orange BookSPLATC N05BB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeN05BB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc1172789216044 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-04)
- ndc11727892161212 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-12)
- ndc11727892162020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-20)
- ndc11727892163030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-30)
- ndc11727892164040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-40)
- ndc11727892166060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-60)
- ndc11727892169090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-90)
Annotations
Orange Book
A088618
AB
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": "72789-216_3caab728-dec4-fe78-e063-6294a90a17ec",
"productndc": "72789-216",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "088618",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Jan 10, 1986"
}
],
"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": "ANDA088618",
"marketing_category": "ANDA",
"nonproprietary_name": "Hydroxyzine Hydrochloride",
"start_marketing_date": "20121009",
"active_numerator_strength": "25"
}Related drugs
Other records sharing ATC code N05BB01.
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