Oxycodone Hydrochloride

In shortageOrange BookUNIISPLATC N02AA05

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN02AA05

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133506771
60 TABLET in 1 BOTTLE (71335-0677-1)
ndc11
7133506772
90 TABLET in 1 BOTTLE (71335-0677-2)
ndc11
7133506773
120 TABLET in 1 BOTTLE (71335-0677-3)
ndc11
7133506774
30 TABLET in 1 BOTTLE (71335-0677-4)
ndc11
7133506775
100 TABLET in 1 BOTTLE (71335-0677-5)
ndc11
7133506776
40 TABLET in 1 BOTTLE (71335-0677-6)
ndc11
7133506777
18 TABLET in 1 BOTTLE (71335-0677-7)
ndc11
7133506778
28 TABLET in 1 BOTTLE (71335-0677-8)

Annotations

UNII (FDA Substance ID)

C1ENJ2TE6C

OXYCODONE HYDROCHLORIDE

RxCUI 82063

Orange Book

A203638

ABABABABAB

DailyMed SPL labels

1 version tracked

FDA shortage

Currently in shortage

Oxycodone Hydrochloride Oral Solution

Raw payload (JSON)

{
  "unii": {
    "unii": "C1ENJ2TE6C",
    "rxcui": "82063",
    "inchikey": "MUZQPDBAOYKNLO-RKXJKUSZSA-N",
    "display_name": "OXYCODONE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "27124cdf-a3e8-474c-9c1e-6fa48f6ddc05": {
      "match": "brand_token",
      "title": "OXYCODONE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK]",
      "spl_version": "102",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-0677_5594265a-34ae-4fc4-b57d-f27189660711",
  "productndc": "71335-0677",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "203638",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Jun 3, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Jun 3, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "003",
        "approval_date": "Jun 3, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "004",
        "approval_date": "Jun 3, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "30MG",
        "product_no": "005",
        "approval_date": "Jun 3, 2014"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "OXYCODONE HYDROCHLORIDE",
  "shortage_reason": "Oxycodone Hydrochloride Oral Solution",
  "shortage_status": "current",
  "proprietary_name": "Oxycodone Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA203638",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Oxycodone",
  "start_marketing_date": "20121030",
  "active_numerator_strength": "30"
}

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