brixadi
Generic: buprenorphine
Labeler: braeburn inc.Drug Facts
Product Profile
Brand Name
brixadi
Generic Name
buprenorphine
Labeler
braeburn inc.
Dosage Form
INJECTION
Routes
Active Ingredients
buprenorphine 128 mg/.36mL
Manufacturer
Identifiers & Regulatory
Product NDC
58284-228
Product ID
58284-228_4e1985eb-1302-42e0-ac79-10b0a492966a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA210136
DEA Schedule
ciii
Listing Expiration
2027-12-31
Marketing Start
2023-06-06
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58284228
Hyphenated Format
58284-228
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
brixadi (source: ndc)
Generic Name
buprenorphine (source: ndc)
Application Number
NDA210136 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 128 mg/.36mL
Packaging
- 1 SYRINGE, GLASS in 1 CARTON (58284-228-01) / .36 mL in 1 SYRINGE, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "4e1985eb-1302-42e0-ac79-10b0a492966a", "openfda": {"nui": ["N0000175689", "N0000175685"], "unii": ["40D3SCR4GZ"], "rxcui": ["2639021", "2639027", "2639029", "2639030", "2639031", "2639032", "2639033", "2639034", "2639036", "2639039", "2639041", "2639042", "2639043", "2639044"], "spl_set_id": ["5d8a8fd0-8619-422a-a664-d1d2e8970f48"], "pharm_class_epc": ["Partial Opioid Agonist [EPC]"], "pharm_class_moa": ["Partial Opioid Agonists [MoA]"], "manufacturer_name": ["Braeburn Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE, GLASS in 1 CARTON (58284-228-01) / .36 mL in 1 SYRINGE, GLASS", "package_ndc": "58284-228-01", "marketing_start_date": "20230606"}], "brand_name": "BRIXADI", "product_id": "58284-228_4e1985eb-1302-42e0-ac79-10b0a492966a", "dosage_form": "INJECTION", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "58284-228", "dea_schedule": "CIII", "generic_name": "BUPRENORPHINE", "labeler_name": "Braeburn Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BRIXADI", "active_ingredients": [{"name": "BUPRENORPHINE", "strength": "128 mg/.36mL"}], "application_number": "NDA210136", "marketing_category": "NDA", "marketing_start_date": "20230606", "listing_expiration_date": "20271231"}