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United States · US · US:47781-410_efb4a6cd-a407-a935-70b9-6ab1074ca819

Hydrocodone Bitartrate

Orange BookUNIISPLATC R05DA03

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

Identification

ManufacturerAlvogen Inc.
CountryUS (United States)
ATC codeR05DA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    4778141060
    60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47781-410-60)

Annotations

UNII (FDA Substance ID)
NO70W886KK
HYDROCODONE BITARTRATE
RxCUI 142439
Orange Book
A206986
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "NO70W886KK",
    "rxcui": "142439",
    "inchikey": "JMBRWJAVUIITGV-LNNMZZBZSA-N",
    "display_name": "HYDROCODONE BITARTRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1f9c1adc-f84f-43de-af5c-d93703aba7f8": {
      "match": "brand_token",
      "title": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [RHODES PHARMACEUTICALS LLC]",
      "spl_version": "20",
      "published_date": "2026-06-01"
    }
  },
  "productid": "47781-410_efb4a6cd-a407-a935-70b9-6ab1074ca819",
  "productndc": "47781-410",
  "dosage_form": "CAPSULE, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "206986",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Jan 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "15MG",
        "product_no": "002",
        "approval_date": "Jan 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Jan 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "30MG",
        "product_no": "004",
        "approval_date": "Jan 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "40MG",
        "product_no": "005",
        "approval_date": "Jan 21, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "50MG",
        "product_no": "006",
        "approval_date": "Jan 21, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "HYDROCODONE BITARTRATE",
  "proprietary_name": "Hydrocodone Bitartrate",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA206986",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Hydrocodone Bitartrate",
  "start_marketing_date": "20200121",
  "active_numerator_strength": "15"
}

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