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United States · US · US:71335-1522_71cd2ab2-dbe2-4c8b-904a-c8ad320181f9

ACETAMINOPHEN AND CODEINE PHOSPHATE

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
    7133515220
    40 TABLET in 1 BOTTLE (71335-1522-0)
  • ndc11
    7133515221
    6 TABLET in 1 BOTTLE (71335-1522-1)
  • ndc11
    7133515222
    20 TABLET in 1 BOTTLE (71335-1522-2)
  • ndc11
    7133515223
    30 TABLET in 1 BOTTLE (71335-1522-3)
  • ndc11
    7133515224
    84 TABLET in 1 BOTTLE (71335-1522-4)
  • ndc11
    7133515225
    15 TABLET in 1 BOTTLE (71335-1522-5)
  • ndc11
    7133515226
    120 TABLET in 1 BOTTLE (71335-1522-6)
  • ndc11
    7133515227
    100 TABLET in 1 BOTTLE (71335-1522-7)
  • ndc11
    7133515228
    60 TABLET in 1 BOTTLE (71335-1522-8)
  • ndc11
    7133515229
    90 TABLET in 1 BOTTLE (71335-1522-9)

Annotations

UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
Orange Book
A040419
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": {
    "44520aa1-b63f-4239-e063-6394a90a5e14": {
      "match": "brand_token",
      "title": "ACETAMINOPHEN LIQUID / ACETAMINOPHEN DIPHENHYDRAMINE HCL LIQUID (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) KIT [KROGER]",
      "spl_version": "2",
      "published_date": "2026-06-02"
    }
  },
  "productid": "71335-1522_71cd2ab2-dbe2-4c8b-904a-c8ad320181f9",
  "productndc": "71335-1522",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "040419",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AA",
        "strength": "300MG;15MG",
        "product_no": "001",
        "approval_date": "May 31, 2001"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AA",
        "strength": "300MG;30MG",
        "product_no": "002",
        "approval_date": "May 31, 2001"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AA",
        "strength": "300MG;60MG",
        "product_no": "003",
        "approval_date": "May 31, 2001"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACETAMINOPHEN; CODEINE PHOSPHATE",
  "shortage_reason": "Acetaminophen; Oxycodone Hydrochloride Tablet",
  "shortage_status": "current",
  "proprietary_name": "ACETAMINOPHEN AND CODEINE PHOSPHATE",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "ANDA040419",
  "marketing_category": "ANDA",
  "nonproprietary_name": "acetaminophen and codeine phosphate",
  "start_marketing_date": "20010531",
  "active_numerator_strength": "300; 30"
}

Related drugs

Other records sharing ATC code N02BE.

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