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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

  • ndc11
    6362942841
    25 TABLET in 1 BOTTLE (63629-4284-1)
  • ndc11
    6362942842
    60 TABLET in 1 BOTTLE (63629-4284-2)
  • ndc11
    6362942843
    30 TABLET in 1 BOTTLE (63629-4284-3)
  • ndc11
    6362942844
    28 TABLET in 1 BOTTLE (63629-4284-4)
  • ndc11
    6362942845
    90 TABLET in 1 BOTTLE (63629-4284-5)
  • ndc11
    6362942846
    120 TABLET in 1 BOTTLE (63629-4284-6)
  • ndc11
    6362942847
    40 TABLET in 1 BOTTLE (63629-4284-7)
  • ndc11
    6362942848
    20 TABLET in 1 BOTTLE (63629-4284-8)
  • ndc11
    6362942849
    10 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

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