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
43063-903-20	43063-903	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181108	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-20)
43063-903-24	43063-903	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20190225	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	24 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-24)
43063-903-28	43063-903	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181108	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	28 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-28)
43063-903-30	43063-903	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181114	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-30)
43063-905-14	43063-905	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181108	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	14 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-14)
43063-905-20	43063-905	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181108	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-20)
43063-905-30	43063-905	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181108	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-30)
43063-905-40	43063-905	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181112	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	40 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-40)
43063-905-60	43063-905	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20190109	N/A	ANDA	ANDA209312	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-60)
71205-068-20	71205-068	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180801	N/A	ANDA	ANDA209312	Proficient Rx LP	METHOCARBAMOL	750 mg/1	20 TABLET, COATED in 1 BOTTLE (71205-068-20)
71205-068-30	71205-068	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	Proficient Rx LP	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE (71205-068-30)
71205-068-40	71205-068	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	Proficient Rx LP	METHOCARBAMOL	750 mg/1	40 TABLET, COATED in 1 BOTTLE (71205-068-40)
71205-068-45	71205-068	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180801	N/A	ANDA	ANDA209312	Proficient Rx LP	METHOCARBAMOL	750 mg/1	45 TABLET, COATED in 1 BOTTLE (71205-068-45)
71205-068-60	71205-068	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180801	N/A	ANDA	ANDA209312	Proficient Rx LP	METHOCARBAMOL	750 mg/1	60 TABLET, COATED in 1 BOTTLE (71205-068-60)
71205-068-90	71205-068	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180801	N/A	ANDA	ANDA209312	Proficient Rx LP	METHOCARBAMOL	750 mg/1	90 TABLET, COATED in 1 BOTTLE (71205-068-90)