美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
69844-086-01	69844-086	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20240110	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	20 mg/1	30 TABLET in 1 BOTTLE (69844-086-01)
69844-086-02	69844-086	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20240110	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	20 mg/1	100 TABLET in 1 BOTTLE (69844-086-02)
69844-086-03	69844-086	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20240110	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	20 mg/1	1000 TABLET in 1 BOTTLE (69844-086-03)
69844-085-01	69844-085	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20240110	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	10 mg/1	30 TABLET in 1 BOTTLE (69844-085-01)
69844-085-02	69844-085	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20240110	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	10 mg/1	100 TABLET in 1 BOTTLE (69844-085-02)
69844-085-03	69844-085	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20240110	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	10 mg/1	1000 TABLET in 1 BOTTLE (69844-085-03)
69844-135-01	69844-135	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20241024	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	5 mg/1	30 TABLET in 1 BOTTLE (69844-135-01)
69844-135-02	69844-135	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20241024	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	5 mg/1	100 TABLET in 1 BOTTLE (69844-135-02)
69844-135-03	69844-135	HUMAN PRESCRIPTION DRUG	BACLOFEN	baclofen	TABLET	ORAL	20241024	N/A	ANDA	ANDA217788	Graviti Pharmaceuticals Private Limited	BACLOFEN	5 mg/1	1000 TABLET in 1 BOTTLE (69844-135-03)