美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=BUPRENORPHINE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
BUPRENORPHINE HYDROCHLORIDE 219401 002 ANDA BUPRENORPHINE HYDROCHLORIDE TABLET;SUBLINGUAL EQ 8MG BASE No No 2025/12/18 2025/12/18 ASCENT PHARMS INC Prescription
BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE 219850 001 ANDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 2MG BASE;EQ 0.5MG BASE No No 2026/01/21 -- ASCENT PHARMS INC Prescription
BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE 219850 002 ANDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 4MG BASE;EQ 1MG BASE No No 2026/01/21 -- ASCENT PHARMS INC Prescription
BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE 219850 003 ANDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 8MG BASE;EQ 2MG BASE No No 2026/01/21 -- ASCENT PHARMS INC Prescription
BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE 219850 004 ANDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 12MG BASE;EQ 3MG BASE No No 2026/01/21 -- ASCENT PHARMS INC Prescription
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