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United States · US · US:71335-2060_96e8ca65-5865-49f0-a3b9-d1ed9da93648
Buspirone Hydrochloride
Orange BookUNIISPLATC N05BE01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN05BE01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc11713352060130 TABLET in 1 BOTTLE, PLASTIC (71335-2060-1)
- ndc117133520602100 TABLET in 1 BOTTLE, PLASTIC (71335-2060-2)
- ndc11713352060360 TABLET in 1 BOTTLE, PLASTIC (71335-2060-3)
- ndc11713352060490 TABLET in 1 BOTTLE, PLASTIC (71335-2060-4)
- ndc117133520605120 TABLET in 1 BOTTLE, PLASTIC (71335-2060-5)
- ndc11713352060628 TABLET in 1 BOTTLE, PLASTIC (71335-2060-6)
- ndc117133520607180 TABLET in 1 BOTTLE, PLASTIC (71335-2060-7)
Annotations
UNII (FDA Substance ID)
207LT9J9OC
BUSPIRONE HYDROCHLORIDE
RxCUI 203116
Orange Book
A210907
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "207LT9J9OC",
"rxcui": "203116",
"inchikey": "RICLFGYGYQXUFH-UHFFFAOYSA-N",
"display_name": "BUSPIRONE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"2c516eec-65d9-4481-8823-ae6b6da84062": {
"match": "brand_token",
"title": "BUSPIRONE HYDROCHLORIDE TABLET [IPG PHARMACEUTICALS, INC]",
"spl_version": "2",
"published_date": "2026-06-02"
}
},
"productid": "71335-2060_96e8ca65-5865-49f0-a3b9-d1ed9da93648",
"productndc": "71335-2060",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "210907",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Nov 14, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "002",
"approval_date": "Nov 14, 2019"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "003",
"approval_date": "Nov 14, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "30MG",
"product_no": "004",
"approval_date": "Nov 14, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BUSPIRONE HYDROCHLORIDE",
"proprietary_name": "Buspirone Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210907",
"marketing_category": "ANDA",
"nonproprietary_name": "Buspirone Hydrochloride",
"start_marketing_date": "20191114",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code N05BE01.
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