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United States · US · US:0172-3927_db225e5f-9265-4460-ab58-3305246c6258
Diazepam
Orange BookUNIISPLATC N05BA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeN05BA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc110172392760100 TABLET in 1 BOTTLE (0172-3927-60)
- ndc110172392770500 TABLET in 1 BOTTLE (0172-3927-70)
- ndc1101723927801000 TABLET in 1 BOTTLE (0172-3927-80)
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": "0172-3927_db225e5f-9265-4460-ab58-3305246c6258",
"productndc": "0172-3927",
"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
Other records sharing ATC code N05BA01.
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