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
72789-041-60	72789-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191219	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)
72789-041-20	72789-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200213	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)
72789-041-30	72789-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200116	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)
72789-110-40	72789-110	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200908	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40)
71205-103-45	71205-103	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA208507	Proficient Rx LP	METHOCARBAMOL	500 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71205-103-45)
71205-103-60	71205-103	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA208507	Proficient Rx LP	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-103-60)
71205-103-90	71205-103	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA208507	Proficient Rx LP	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-103-90)
53002-3041-6	53002-3041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20220701	N/A	ANDA	ANDA208507	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-3041-6)
71205-103-20	71205-103	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA208507	Proficient Rx LP	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-103-20)
71205-103-30	71205-103	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA208507	Proficient Rx LP	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-103-30)
71205-103-40	71205-103	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA208507	Proficient Rx LP	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71205-103-40)
53002-3041-1	53002-3041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20220701	N/A	ANDA	ANDA208507	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (53002-3041-1)
53002-3041-2	53002-3041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20220701	N/A	ANDA	ANDA208507	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (53002-3041-2)
53002-3041-3	53002-3041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20220701	N/A	ANDA	ANDA208507	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-3041-3)