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United States · US · US:68071-2471_136a6ad3-3965-ca75-e063-6394a90a15f9

Cyclobenzaprine hydrochloride

Orange BookUNIISPLATC M03BX08

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

Identification

ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeM03BX08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6807124711
    15 TABLET, FILM COATED in 1 BOTTLE (68071-2471-1)
  • ndc11
    6807124712
    20 TABLET, FILM COATED in 1 BOTTLE (68071-2471-2)
  • ndc11
    6807124717
    21 TABLET, FILM COATED in 1 BOTTLE (68071-2471-7)
  • ndc11
    6807124719
    90 TABLET, FILM COATED in 1 BOTTLE (68071-2471-9)

Annotations

UNII (FDA Substance ID)
0VE05JYS2P
CYCLOBENZAPRINE HYDROCHLORIDE
RxCUI 52101
Orange Book
A213324
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "0VE05JYS2P",
    "rxcui": "52101",
    "inchikey": "VXEAYBOGHINOKW-UHFFFAOYSA-N",
    "display_name": "CYCLOBENZAPRINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "fe81c68d-a579-4fe9-e053-6294a90a7bc0": {
      "match": "brand_token",
      "title": "CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY]",
      "spl_version": "8",
      "published_date": "2026-06-01"
    }
  },
  "productid": "68071-2471_136a6ad3-3965-ca75-e063-6394a90a15f9",
  "productndc": "68071-2471",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "213324",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Jul 6, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "002",
        "approval_date": "Jul 6, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "003",
        "approval_date": "Jul 5, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CYCLOBENZAPRINE HYDROCHLORIDE",
  "proprietary_name": "Cyclobenzaprine hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA213324",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Cyclobenzaprine hydrochloride",
  "start_marketing_date": "20200706",
  "active_numerator_strength": "7.5"
}

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