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United States · US · US:0409-2012_37d2deb6-c54a-42bb-ad76-4873a59da562
Buprenorphine Hydrochloride
Orange BookUNIISPLATC N07BC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHospira, Inc.
CountryUS (United States)
ATC codeN07BC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11040920123210 CARTRIDGE in 1 CARTON (0409-2012-32) / 1 mL in 1 CARTRIDGE (0409-2012-03)
Annotations
UNII (FDA Substance ID)
56W8MW3EN1
BUPRENORPHINE HYDROCHLORIDE
RxCUI 203841
Orange Book
A074137
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "56W8MW3EN1",
"rxcui": "203841",
"inchikey": "UAIXRPCCYXNJMQ-RZIPZOSSSA-N",
"display_name": "BUPRENORPHINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAMUSCULAR; INTRAVENOUS",
"spl_meta": {
"2738feae-316e-426f-971c-5f142ac01b60": {
"match": "brand_token",
"title": "BUPRENORPHINE PATCH [RHODES PHARMACEUTICALS LLC]",
"spl_version": "17",
"published_date": "2026-06-01"
}
},
"productid": "0409-2012_37d2deb6-c54a-42bb-ad76-4873a59da562",
"productndc": "0409-2012",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "074137",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 0.3MG BASE/ML",
"product_no": "001",
"approval_date": "Jun 3, 1996"
}
],
"appl_type": "A"
},
"dea_schedule": "CIII",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BUPRENORPHINE HYDROCHLORIDE",
"proprietary_name": "Buprenorphine Hydrochloride",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA074137",
"marketing_category": "ANDA",
"nonproprietary_name": "Buprenorphine Hydrochloride",
"start_marketing_date": "20050614",
"active_numerator_strength": ".3"
}Related drugs
Other records sharing ATC code N07BC01.
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