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)
检索条件:" 注册申请号=ANDA204872"
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
68071-5039-1 68071-5039 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20230110 N/A ANDA ANDA204872 NuCare Pharmaceuticals,Inc. NAPROXEN SODIUM 220 mg/1 21 TABLET in 1 BOTTLE (68071-5039-1)
66715-5428-4 66715-5428 HUMAN OTC DRUG 24/7 Life by 7-Eleven Naproxen Sodium naproxen sodium tablet, film coated TABLET, FILM COATED ORAL 20220419 N/A ANDA ANDA204872 Lil' Drug Store Products, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (66715-5428-4) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-4170-5 11822-4170 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220707 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-4170-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-471-11 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 60 POUCH in 1 CARTON (50844-471-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)
50844-471-14 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-14)
50844-471-16 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-16)
50844-471-19 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (50844-471-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-471-22 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 48 POUCH in 1 CARTON (50844-471-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)
53185-604-12 53185-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220311 N/A ANDA ANDA204872 Athlete's Needs Inc NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53185-604-12)
53185-604-15 53185-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220311 N/A ANDA ANDA204872 Athlete's Needs Inc NAPROXEN SODIUM 220 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53185-604-15)
71141-182-32 71141-182 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20230522 N/A ANDA ANDA204872 Lidl US LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (71141-182-32) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
51316-817-08 51316-817 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220418 N/A ANDA ANDA204872 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (51316-817-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
51316-817-52 51316-817 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220418 N/A ANDA ANDA204872 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (51316-817-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-4171-5 11822-4171 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220707 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-4171-5) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-604-06 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20260219 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-06)
50844-604-09 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 4 BLISTER PACK in 1 CARTON (50844-604-09) / 5 TABLET, FILM COATED in 1 BLISTER PACK
50844-471-56 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-56)
50844-471-98 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-98)
50844-471-99 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-99)
46122-564-71 46122-564 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 Amerisource Bergen NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (46122-564-71) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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