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United States · US · US:71335-1584_dc33c03b-c55f-4b37-9b2b-85c949d2a1c3

Diazepam

Orange BookUNIISPLATC N05BA01

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN05BA01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133515840
    120 TABLET in 1 BOTTLE (71335-1584-0)
  • ndc11
    7133515841
    12 TABLET in 1 BOTTLE (71335-1584-1)
  • ndc11
    7133515842
    15 TABLET in 1 BOTTLE (71335-1584-2)
  • ndc11
    7133515843
    20 TABLET in 1 BOTTLE (71335-1584-3)
  • ndc11
    7133515844
    30 TABLET in 1 BOTTLE (71335-1584-4)
  • ndc11
    7133515845
    60 TABLET in 1 BOTTLE (71335-1584-5)
  • ndc11
    7133515846
    90 TABLET in 1 BOTTLE (71335-1584-6)
  • ndc11
    7133515847
    10 TABLET in 1 BOTTLE (71335-1584-7)
  • ndc11
    7133515848
    2 TABLET in 1 BOTTLE (71335-1584-8)
  • ndc11
    7133515849
    1 TABLET in 1 BOTTLE (71335-1584-9)

Annotations

UNII (FDA Substance ID)
Q3JTX2Q7TU
DIAZEPAM
RxCUI 3322
Orange Book
A071321
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": "71335-1584_dc33c03b-c55f-4b37-9b2b-85c949d2a1c3",
  "productndc": "71335-1584",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "071321",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "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": "ANDA071321",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diazepam",
  "start_marketing_date": "19861210",
  "active_numerator_strength": "5"
}

Related drugs

Other records sharing ATC code N05BA01.

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