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United States · US · US:76420-784_2cb3e981-e5b2-9d49-e063-6394a90abfbd

Diazepam

Orange BookUNIISPLATC N05BA01

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

Identification

ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeN05BA01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 11

  • ndc11
    7642078400
    1000 TABLET in 1 BOTTLE (76420-784-00)
  • ndc11
    7642078401
    100 TABLET in 1 BOTTLE (76420-784-01)
  • ndc11
    7642078402
    2 TABLET in 1 BOTTLE (76420-784-02)
  • ndc11
    7642078403
    3 TABLET in 1 BOTTLE (76420-784-03)
  • ndc11
    7642078405
    5 TABLET in 1 BOTTLE (76420-784-05)
  • ndc11
    7642078410
    10 TABLET in 1 BOTTLE (76420-784-10)
  • ndc11
    7642078420
    20 TABLET in 1 BOTTLE (76420-784-20)
  • ndc11
    7642078430
    30 TABLET in 1 BOTTLE (76420-784-30)
  • ndc11
    7642078455
    500 TABLET in 1 BOTTLE (76420-784-55)
  • ndc11
    7642078460
    60 TABLET in 1 BOTTLE (76420-784-60)
  • ndc11
    7642078490
    90 TABLET in 1 BOTTLE (76420-784-90)

Annotations

UNII (FDA Substance ID)
Q3JTX2Q7TU
DIAZEPAM
RxCUI 3322
Orange Book
A071322
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "Q3JTX2Q7TU",
    "rxcui": "3322",
    "inchikey": "AAOVKJBEBIDNHE-UHFFFAOYSA-N",
    "display_name": "DIAZEPAM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7e7dd743-a87b-4ab3-b6ae-f116cd0c8b0f": {
      "match": "brand_token",
      "title": "DIAZEPAM INJECTION, SOLUTION [HOSPIRA, INC.]",
      "spl_version": "26",
      "published_date": "2026-05-25"
    }
  },
  "productid": "76420-784_2cb3e981-e5b2-9d49-e063-6394a90abfbd",
  "productndc": "76420-784",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "071322",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Dec 10, 1986"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIV",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DIAZEPAM",
  "proprietary_name": "Diazepam",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA071322",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diazepam",
  "start_marketing_date": "19861210",
  "active_numerator_strength": "10"
}

Related drugs

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