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United States · US · US:71335-2306_b9906136-3102-42b2-9599-7109a9a41f0f
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
- ndc11713352306056 TABLET in 1 BOTTLE, PLASTIC (71335-2306-0)
- ndc11713352306120 TABLET in 1 BOTTLE, PLASTIC (71335-2306-1)
- ndc11713352306230 TABLET in 1 BOTTLE, PLASTIC (71335-2306-2)
- ndc11713352306340 TABLET in 1 BOTTLE, PLASTIC (71335-2306-3)
- ndc11713352306450 TABLET in 1 BOTTLE, PLASTIC (71335-2306-4)
- ndc11713352306560 TABLET in 1 BOTTLE, PLASTIC (71335-2306-5)
- ndc11713352306690 TABLET in 1 BOTTLE, PLASTIC (71335-2306-6)
- ndc117133523067100 TABLET in 1 BOTTLE, PLASTIC (71335-2306-7)
- ndc11713352306810 TABLET in 1 BOTTLE, PLASTIC (71335-2306-8)
- ndc117133523069120 TABLET in 1 BOTTLE, PLASTIC (71335-2306-9)
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": "71335-2306_b9906136-3102-42b2-9599-7109a9a41f0f",
"productndc": "71335-2306",
"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": "10"
}Related drugs
Other records sharing ATC code N05BA01.
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