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 · 10

ndc11
7133509810
15 TABLET in 1 BOTTLE (71335-0981-0)
ndc11
7133509811
30 TABLET in 1 BOTTLE (71335-0981-1)
ndc11
7133509812
60 TABLET in 1 BOTTLE (71335-0981-2)
ndc11
7133509813
90 TABLET in 1 BOTTLE (71335-0981-3)
ndc11
7133509814
56 TABLET in 1 BOTTLE (71335-0981-4)
ndc11
7133509815
100 TABLET in 1 BOTTLE (71335-0981-5)
ndc11
7133509816
120 TABLET in 1 BOTTLE (71335-0981-6)
ndc11
7133509817
50 TABLET in 1 BOTTLE (71335-0981-7)
ndc11
7133509818
40 TABLET in 1 BOTTLE (71335-0981-8)
ndc11
7133509819
20 TABLET in 1 BOTTLE (71335-0981-9)

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": "71335-0981_dca003cc-0feb-46b3-aedc-73c20fc7f798",
  "productndc": "71335-0981",
  "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": "5"
}

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