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
87063-040-30	87063-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (87063-040-30)
87063-040-60	87063-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (87063-040-60)
87063-040-90	87063-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (87063-040-90)
87063-041-01	87063-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (87063-041-01)
87063-041-10	87063-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (87063-041-10)
87063-041-20	87063-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (87063-041-20)
87063-041-30	87063-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (87063-041-30)
87063-041-60	87063-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (87063-041-60)
87063-041-90	87063-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (87063-041-90)
87063-040-20	87063-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (87063-040-20)
87063-040-10	87063-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (87063-040-10)
87063-040-01	87063-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA213967	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (87063-040-01)
85509-1341-3	85509-1341	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250729	N/A	ANDA	ANDA213967	PHOENIX RX LLC	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85509-1341-3)
85509-1341-6	85509-1341	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250729	N/A	ANDA	ANDA213967	PHOENIX RX LLC	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85509-1341-6)
71335-2794-2	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2794-2)
71335-2794-4	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2794-4)
71335-2794-5	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2794-5)
71335-2794-6	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-2794-6)
71335-2794-7	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2794-7)
71335-2794-8	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2794-8)