Package 70069-027-05

Brand: buprenorphine hydrochloride

Generic: buprenorphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-027-05
Digits Only 7006902705
Product NDC 70069-027
Product ID 70069-027_abc53fa8-3d75-47b5-bfb1-d61872c1ddb4
Description

5 VIAL in 1 CARTON (70069-027-05) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-02-11
Brand buprenorphine hydrochloride
Generic buprenorphine hydrochloride
Sample Package No

Linked Drug Pages (1)

Buprenorphine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "abc53fa8-3d75-47b5-bfb1-d61872c1ddb4", "openfda": {"upc": ["0370069027059", "0370069027011"], "unii": ["56W8MW3EN1"], "rxcui": ["238129"], "spl_set_id": ["74e40c51-853b-4e7f-b3cb-a27af29e1cbf"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (70069-027-05)  / 1 mL in 1 VIAL", "package_ndc": "70069-027-05", "marketing_start_date": "20250211"}], "brand_name": "Buprenorphine Hydrochloride", "product_id": "70069-027_abc53fa8-3d75-47b5-bfb1-d61872c1ddb4", "dosage_form": "INJECTION", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "70069-027", "dea_schedule": "CIII", "generic_name": "Buprenorphine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine Hydrochloride", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": ".324 mg/mL"}], "application_number": "ANDA219302", "marketing_category": "ANDA", "marketing_start_date": "20250211", "listing_expiration_date": "20261231"}