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United States · US · US:71335-2239_a4623d8d-0257-43db-bd8a-be652068231a
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
- ndc117133522390120 TABLET in 1 BOTTLE, PLASTIC (71335-2239-0)
- ndc11713352239112 TABLET in 1 BOTTLE, PLASTIC (71335-2239-1)
- ndc11713352239215 TABLET in 1 BOTTLE, PLASTIC (71335-2239-2)
- ndc11713352239320 TABLET in 1 BOTTLE, PLASTIC (71335-2239-3)
- ndc11713352239430 TABLET in 1 BOTTLE, PLASTIC (71335-2239-4)
- ndc11713352239560 TABLET in 1 BOTTLE, PLASTIC (71335-2239-5)
- ndc11713352239690 TABLET in 1 BOTTLE, PLASTIC (71335-2239-6)
- ndc11713352239710 TABLET in 1 BOTTLE, PLASTIC (71335-2239-7)
- ndc1171335223982 TABLET in 1 BOTTLE, PLASTIC (71335-2239-8)
- ndc1171335223991 TABLET in 1 BOTTLE, PLASTIC (71335-2239-9)
Annotations
UNII (FDA Substance ID)
Q3JTX2Q7TU
DIAZEPAM
RxCUI 3322
Orange Book
A070325
ABABAB
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": "71335-2239_a4623d8d-0257-43db-bd8a-be652068231a",
"productndc": "71335-2239",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "070325",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "001",
"approval_date": "Sep 4, 1985"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2MG",
"product_no": "002",
"approval_date": "Sep 4, 1985"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "003",
"approval_date": "Sep 4, 1985"
}
],
"appl_type": "A"
},
"dea_schedule": "CIV",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIAZEPAM",
"proprietary_name": "Diazepam",
"active_ingred_unit": "mg/1",
"application_number": "ANDA070325",
"marketing_category": "ANDA",
"nonproprietary_name": "diazepam",
"start_marketing_date": "19850904",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code N05BA01.
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