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United States · US · US:71335-0316_68226f26-8369-4b58-a0e9-e9b943a8df09

Oxycodone and Acetaminophen

In shortageOrange BookUNIISPLATC N02BE

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN02BE
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133503160
    84 TABLET in 1 BOTTLE (71335-0316-0)
  • ndc11
    7133503161
    120 TABLET in 1 BOTTLE (71335-0316-1)
  • ndc11
    7133503162
    90 TABLET in 1 BOTTLE (71335-0316-2)
  • ndc11
    7133503163
    60 TABLET in 1 BOTTLE (71335-0316-3)
  • ndc11
    7133503164
    30 TABLET in 1 BOTTLE (71335-0316-4)
  • ndc11
    7133503165
    100 TABLET in 1 BOTTLE (71335-0316-5)
  • ndc11
    7133503166
    45 TABLET in 1 BOTTLE (71335-0316-6)
  • ndc11
    7133503167
    28 TABLET in 1 BOTTLE (71335-0316-7)
  • ndc11
    7133503168
    168 TABLET in 1 BOTTLE (71335-0316-8)
  • ndc11
    7133503169
    20 TABLET in 1 BOTTLE (71335-0316-9)

Annotations

UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
Orange Book
A202677
AAAAAA
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Acetaminophen; Oxycodone Hydrochloride Tablet
Raw payload (JSON)
{
  "unii": {
    "unii": "362O9ITL9D",
    "rxcui": "161",
    "inchikey": "RZVAJINKPMORJF-UHFFFAOYSA-N",
    "display_name": "ACETAMINOPHEN",
    "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": "71335-0316_68226f26-8369-4b58-a0e9-e9b943a8df09",
  "productndc": "71335-0316",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202677",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "325MG;7.5MG",
        "product_no": "001",
        "approval_date": "Jul 26, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "325MG;10MG",
        "product_no": "002",
        "approval_date": "Jul 26, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "325MG;5MG",
        "product_no": "003",
        "approval_date": "Mar 8, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE",
  "shortage_reason": "Acetaminophen; Oxycodone Hydrochloride Tablet",
  "shortage_status": "current",
  "proprietary_name": "Oxycodone and Acetaminophen",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "ANDA202677",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Oxycodone and Acetaminophen",
  "start_marketing_date": "20120117",
  "active_numerator_strength": "325; 7.5"
}

Related drugs

Other records sharing ATC code N02BE.

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