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United States · US · US:71335-0723_dd7057dd-4448-4f11-8c2d-6a1bfe0e1f50

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 · 10

  • ndc11
    7133507230
    90 TABLET in 1 BOTTLE (71335-0723-0)
  • ndc11
    7133507231
    30 TABLET in 1 BOTTLE (71335-0723-1)
  • ndc11
    7133507232
    180 TABLET in 1 BOTTLE (71335-0723-2)
  • ndc11
    7133507233
    120 TABLET in 1 BOTTLE (71335-0723-3)
  • ndc11
    7133507234
    20 TABLET in 1 BOTTLE (71335-0723-4)
  • ndc11
    7133507235
    25 TABLET in 1 BOTTLE (71335-0723-5)
  • ndc11
    7133507236
    100 TABLET in 1 BOTTLE (71335-0723-6)
  • ndc11
    7133507237
    60 TABLET in 1 BOTTLE (71335-0723-7)
  • ndc11
    7133507238
    56 TABLET in 1 BOTTLE (71335-0723-8)
  • ndc11
    7133507239
    140 TABLET in 1 BOTTLE (71335-0723-9)

Annotations

UNII (FDA Substance ID)
L960UP2KRW
HYDROMORPHONE HYDROCHLORIDE
RxCUI 203177
Orange Book
A205814
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": "71335-0723_dd7057dd-4448-4f11-8c2d-6a1bfe0e1f50",
  "productndc": "71335-0723",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "205814",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2MG",
        "product_no": "001",
        "approval_date": "May 13, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "4MG",
        "product_no": "002",
        "approval_date": "May 13, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "8MG",
        "product_no": "003",
        "approval_date": "May 13, 2016"
      }
    ],
    "appl_type": "A"
  },
  "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": "ANDA205814",
  "marketing_category": "ANDA",
  "nonproprietary_name": "HYDROMORPHONE HYDROCHLORIDE",
  "start_marketing_date": "20160517",
  "active_numerator_strength": "4"
}

Related drugs

Other records sharing ATC code N02AA03.

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