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United States · US · US:63629-4284_07884a78-2a01-453c-870b-7b757b530d22
Hydromorphone Hydrochloride
In shortageOrange BookUNIISPLATC N02AA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN02AA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc11636294284125 TABLET in 1 BOTTLE (63629-4284-1)
- ndc11636294284260 TABLET in 1 BOTTLE (63629-4284-2)
- ndc11636294284330 TABLET in 1 BOTTLE (63629-4284-3)
- ndc11636294284428 TABLET in 1 BOTTLE (63629-4284-4)
- ndc11636294284590 TABLET in 1 BOTTLE (63629-4284-5)
- ndc116362942846120 TABLET in 1 BOTTLE (63629-4284-6)
- ndc11636294284740 TABLET in 1 BOTTLE (63629-4284-7)
- ndc11636294284820 TABLET in 1 BOTTLE (63629-4284-8)
- ndc11636294284910 TABLET in 1 BOTTLE (63629-4284-9)
Annotations
UNII (FDA Substance ID)
L960UP2KRW
HYDROMORPHONE HYDROCHLORIDE
RxCUI 203177
Orange Book
N019892
ABABAB
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Hydromorphone Hydrochloride Injection
Raw payload (JSON)
{
"unii": {
"unii": "L960UP2KRW",
"rxcui": "203177",
"inchikey": "XHILEZUETWRSHC-NRGUFEMZSA-N",
"display_name": "HYDROMORPHONE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"37565441-0d95-4743-a695-d7b3326f58a1": {
"match": "brand_token",
"title": "HYDROMORPHONE HYDROCHLORIDE TABLET HYDROMORPHONE HYDROCHLORIDE SOLUTION [RHODES PHARMACEUTICALS LLC]",
"spl_version": "20",
"published_date": "2026-05-20"
}
},
"productid": "63629-4284_07884a78-2a01-453c-870b-7b757b530d22",
"productndc": "63629-4284",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "019892",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "8MG",
"product_no": "001",
"approval_date": "Dec 7, 1992"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "4MG",
"product_no": "002",
"approval_date": "Nov 9, 2007"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "2MG",
"product_no": "003",
"approval_date": "Nov 9, 2007"
}
],
"appl_type": "N"
},
"dea_schedule": "CII",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "HYDROMORPHONE HYDROCHLORIDE",
"shortage_reason": "Hydromorphone Hydrochloride Injection",
"shortage_status": "current",
"proprietary_name": "Hydromorphone Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "NDA019892",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Hydromorphone Hydrochloride",
"start_marketing_date": "20091123",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code N02AA03.
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