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
71335-0300-9	71335-0300	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride	TABLET	ORAL	20190503	N/A	ANDA	ANDA077829	Bryant Ranch Prepack	CETIRIZINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (71335-0300-9)
70677-1241-1	70677-1241	HUMAN OTC DRUG	Allergy Relief	Cetirizine Hydrochloride	TABLET, FILM COATED	ORAL	20240124	N/A	ANDA	ANDA077829	Strategic Sourcing Services LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (70677-1241-1)
70692-180-14	70692-180	HUMAN OTC DRUG	RIGHT REMEDIES ALL-DAY Allergy Relief	Cetirizine Hydrochloride	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA077829	Strive Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	1 BOTTLE in 1 CARTON (70692-180-14) / 14 TABLET, FILM COATED in 1 BOTTLE
70692-180-31	70692-180	HUMAN OTC DRUG	RIGHT REMEDIES ALL-DAY Allergy Relief	Cetirizine Hydrochloride	TABLET, FILM COATED	ORAL	20251124	N/A	ANDA	ANDA077829	Strive Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	300 TABLET, FILM COATED in 1 BOTTLE (70692-180-31)
60760-886-30	60760-886	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride	TABLET	ORAL	20230117	N/A	ANDA	ANDA077829	ST. MARY'S MEDICAL PARK PHARMACY	CETIRIZINE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-886-30)
84324-001-01	84324-001	HUMAN OTC DRUG	Allergy Relief	Cetirizine HCl	TABLET	ORAL	20240717	N/A	ANDA	ANDA077829	NUVICARE LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (84324-001-01)
84324-001-02	84324-001	HUMAN OTC DRUG	Allergy Relief	Cetirizine HCl	TABLET	ORAL	20250609	N/A	ANDA	ANDA077829	NUVICARE LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	14 TABLET in 1 BLISTER PACK (84324-001-02)
85293-001-01	85293-001	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride	TABLET	ORAL	20250304	N/A	ANDA	ANDA077829	Umasuto, LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (85293-001-01)