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United States · US · US:71335-9674_2b832254-e7b8-4d1a-9775-cdcffce01451

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
    7133596740
    25 TABLET in 1 BOTTLE (71335-9674-0)
  • ndc11
    7133596741
    10 TABLET in 1 BOTTLE (71335-9674-1)
  • ndc11
    7133596742
    120 TABLET in 1 BOTTLE (71335-9674-2)
  • ndc11
    7133596743
    28 TABLET in 1 BOTTLE (71335-9674-3)
  • ndc11
    7133596744
    12 TABLET in 1 BOTTLE (71335-9674-4)
  • ndc11
    7133596745
    40 TABLET in 1 BOTTLE (71335-9674-5)
  • ndc11
    7133596746
    30 TABLET in 1 BOTTLE (71335-9674-6)
  • ndc11
    7133596747
    90 TABLET in 1 BOTTLE (71335-9674-7)
  • ndc11
    7133596748
    60 TABLET in 1 BOTTLE (71335-9674-8)
  • ndc11
    7133596749
    84 TABLET in 1 BOTTLE (71335-9674-9)

Annotations

UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
Orange Book
A207510
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": "71335-9674_2b832254-e7b8-4d1a-9775-cdcffce01451",
  "productndc": "71335-9674",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "207510",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "325MG;5MG",
        "product_no": "001",
        "approval_date": "Mar 21, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "325MG;7.5MG",
        "product_no": "002",
        "approval_date": "Mar 21, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "325MG;10MG",
        "product_no": "003",
        "approval_date": "Mar 21, 2018"
      }
    ],
    "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": "ANDA207510",
  "marketing_category": "ANDA",
  "nonproprietary_name": "oxycodone and acetaminophen",
  "start_marketing_date": "20190601",
  "active_numerator_strength": "325; 5"
}

Related drugs

Other records sharing ATC code N02BE.

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