Hydromorphone Hydrochloride

In shortageOrange BookUNIISPLATC N02AA03

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

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
7133597010
90 TABLET in 1 BOTTLE, PLASTIC (71335-9701-0)
ndc11
7133597011
30 TABLET in 1 BOTTLE, PLASTIC (71335-9701-1)
ndc11
7133597012
180 TABLET in 1 BOTTLE, PLASTIC (71335-9701-2)
ndc11
7133597013
120 TABLET in 1 BOTTLE, PLASTIC (71335-9701-3)
ndc11
7133597014
20 TABLET in 1 BOTTLE, PLASTIC (71335-9701-4)
ndc11
7133597015
25 TABLET in 1 BOTTLE, PLASTIC (71335-9701-5)
ndc11
7133597016
100 TABLET in 1 BOTTLE, PLASTIC (71335-9701-6)
ndc11
7133597017
60 TABLET in 1 BOTTLE, PLASTIC (71335-9701-7)
ndc11
7133597018
56 TABLET in 1 BOTTLE, PLASTIC (71335-9701-8)
ndc11
7133597019
140 TABLET in 1 BOTTLE, PLASTIC (71335-9701-9)

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": "71335-9701_b9b96266-fe94-4282-915f-277433e1ca26",
  "productndc": "71335-9701",
  "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": "4"
}

Related drugs

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