| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70518-4529-0 | 70518-4529 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | FOR SUSPENSION | ORAL | 20251202 | N/A | NDA AUTHORIZED GENERIC | NDA050760 | REMEDYREPACK INC. | AMOXICILLIN | 400 mg/5mL | 100 mL in 1 BOTTLE (70518-4529-0) |
| 81964-207-50 | 81964-207 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | FOR SUSPENSION | ORAL | 20240401 | N/A | NDA AUTHORIZED GENERIC | NDA050760 | USAntibiotics, LLC | AMOXICILLIN | 400 mg/5mL | 50 mL in 1 BOTTLE (81964-207-50) |
| 81964-207-51 | 81964-207 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | FOR SUSPENSION | ORAL | 20240401 | N/A | NDA AUTHORIZED GENERIC | NDA050760 | USAntibiotics, LLC | AMOXICILLIN | 400 mg/5mL | 75 mL in 1 BOTTLE (81964-207-51) |
| 81964-207-52 | 81964-207 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | FOR SUSPENSION | ORAL | 20240401 | N/A | NDA AUTHORIZED GENERIC | NDA050760 | USAntibiotics, LLC | AMOXICILLIN | 400 mg/5mL | 100 mL in 1 BOTTLE (81964-207-52) |
| 68071-3925-1 | 68071-3925 | HUMAN PRESCRIPTION DRUG | Amoxicillin | Amoxicillin | FOR SUSPENSION | ORAL | 20251204 | N/A | NDA AUTHORIZED GENERIC | NDA050760 | NuCare Pharmaceuticals, Inc. | AMOXICILLIN | 400 mg/5mL | 100 mL in 1 BOTTLE (68071-3925-1) |