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当前位置:药药网 / 药品 / 美国NDC复合药物数据库文件(本栏目更新到2026-3-31)
药品名称:
商品名称:
药品NDC:
报告期内:
-
格式:2020-5-3
NDC包装id:
市场分类:
不限
ANDA
BLA
NDA
EMERGENCY USE AUTHORIZATION
NDA AUTHORIZED GENERIC
OTC MONOGRAPH FINAL
OTC MONOGRAPH NOT FINAL
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
UNAPPROVED DRUG OTHER
UNAPPROVED HOMEOPATHIC
UNAPPROVED MEDICAL GAS
活性成分:
持证企业:
美国药品NDC(国家药品编码)与药品说明书数据库
美国NDC未完成药物数据库文件
美国NDC复合药物数据库文件
美国NDC 数据库排除药物数据库文件
 美国NDC复合药物数据库文件4843条(本栏目更新到2026-3-31)
药品名称(分析)
商品名
药品NDC
专利人(分析)
报告期内
活性成分
市场分类
规格(分析)
NDC包装id
121022 HYDROCORTISONE 2.5% / IODOQUINOL 1% / KETOCONAZOLE 2%
HUMAN COMPOUNDED DRUG
72934-2370
SKNV
2024-1
KETOCONAZOLE; HYDROCORTISONE; IODOQUINOL
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
2 g/100 mL; 2.5 g/100 mL; 1 g/100 mL
72934-2370-2
Induction 4 to1 High K (50 mEq) In Plasmalyte A, ph 7.4 with Tromethamine 500ml Bag
HUMAN COMPOUNDED DRUG
71285-0111
Central Admixture Pharmacy Services, Inc.
2024-1
MANNITOL; MAGNESIUM SULFATE HEPTAHYDRATE; SODIUM CHLORIDE; POTASSIUM CHLORIDE; MAGNESIUM CHLORIDE; TROMETHAMINE; DEXTROSE MONOHYDRATE; SODIUM ACETATE; SODIUM GLUCONATE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
3.6 g/500 mL; 20.3 meq/500 mL; 1.9725 g/500 mL; 3.86375 g/500 mL; .1125 g/500 mL; 2.268 g/500 mL; 6.51 g/500 mL; 1.38 g/500 mL; 1.8825 g/500 mL
71285-0111-1
Vancomycin 1.75gm added to NS
HUMAN COMPOUNDED DRUG
71285-7060
Central Admixture Pharmacy Services, Inc.
2024-1
VANCOMYCIN HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
1.75 g/500 mL
71285-7060-1
Potassium Phosphate 30mmol added to NS
HUMAN COMPOUNDED DRUG
71285-7016
Central Admixture Pharmacy Services, Inc.
2024-1
POTASSIUM PHOSPHATE, DIBASIC
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
30 mmol/500 mL
71285-7016-1
Oxytocin 30units added to LR
HUMAN COMPOUNDED DRUG
71285-6039
Central Admixture Pharmacy Services, Inc.
2024-1
OXYTOCIN
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
30 [USP'U]/500 mL
71285-6039-1
Trophamine 3% / Dextrose 5% With Calcium Gluconate 3.75mEq and Heparin 125 units 250ml in 250ml bag
HUMAN COMPOUNDED DRUG
72196-0419
Central Admixture Pharmacy Services, Inc.
2024-1
GLUTAMIC ACID; LYSINE ACETATE; SERINE; TYROSINE; N-ACETYLTYROSINE; THREONINE; CYSTEINE HYDROCHLORIDE; HISTIDINE; ARGININE; TAURINE; DEXTROSE MONOHYDRATE; LEUCINE; METHIONINE; PROLINE; ASPARTIC ACID; ISOLEUCINE; ALANINE; GLYCINE; PHENYLALANINE; TRYPTOPHAN; VALINE; CALCIUM GLUCONATE MONOHYDRATE; HEPARIN SODIUM
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
.375 g/250 mL; .9 g/250 mL; .285 g/250 mL; .033 g/250 mL; .18 g/250 mL; .315 g/250 mL; .018 g/250 mL; .36 g/250 mL; .9 g/250 mL; .01875 g/250 mL; 12.5 g/250 mL; 1.05 g/250 mL; .255 g/250 mL; .51 g/250 mL; .24 g/250 mL; .615 g/250 mL; .405 g/250 mL; .27 g/250 mL; .36 g/250 mL; .15 g/250 mL; .585 g/250 mL; 3.75 meq/250 mL; 125 U/250 mL
72196-0419-1
Fentanyl Citrate
HUMAN COMPOUNDED DRUG
73177-102
STAQ Pharma Inc
2024-2
FENTANYL CITRATE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
10 ug/1 mL
73177-102-05
Fentanyl Citrate
HUMAN COMPOUNDED DRUG
73177-102
STAQ Pharma Inc
2024-2
FENTANYL CITRATE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
10 ug/1 mL
73177-102-03
Fentanyl Citrate
HUMAN COMPOUNDED DRUG
73177-102
STAQ Pharma Inc
2024-2
FENTANYL CITRATE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
10 ug/1 mL
73177-102-27
Fentanyl Citrate
HUMAN COMPOUNDED DRUG
73177-102
STAQ Pharma Inc
2024-2
FENTANYL CITRATE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
10 ug/1 mL
73177-102-01
Phenylephrine
HUMAN COMPOUNDED DRUG
73177-108
STAQ Pharma Inc
2024-2
PHENYLEPHRINE HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
100 ug/1 mL
73177-108-03
Ropivacaine
HUMAN COMPOUNDED DRUG
73177-109
STAQ Pharma Inc
2024-2
ROPIVACAINE HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
2 mg/1 mL
73177-109-20
Ropivacaine
HUMAN COMPOUNDED DRUG
73177-109
STAQ Pharma Inc
2024-2
ROPIVACAINE HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
2 mg/1 mL
73177-109-13
Ropivacaine
HUMAN COMPOUNDED DRUG
73177-109
STAQ Pharma Inc
2024-2
ROPIVACAINE HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
2 mg/1 mL
73177-109-26
Ropivacaine
HUMAN COMPOUNDED DRUG
73177-109
STAQ Pharma Inc
2024-2
ROPIVACAINE HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
2 mg/1 mL
73177-109-14
Morphine Sulfate
HUMAN COMPOUNDED DRUG
71449-022
Denver Solutions, LLC dba Leiters Health
2024-2
MORPHINE SULFATE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
5 mg/1 mL
71449-022-32
Ropivacaine Hydrochloride
HUMAN COMPOUNDED DRUG
71449-070
Denver Solutions, LLC dba Leiters Health
2024-2
ROPIVACAINE HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
2 mg/1 mL
71449-070-25
Moxifloxacin
HUMAN COMPOUNDED DRUG
71449-097
Denver Solutions, LLC dba Leiters Health
2024-2
MOXIFLOXACIN HYDROCHLORIDE
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
5 mg/1 mL
71449-097-42
Bevacizumab
HUMAN COMPOUNDED DRUG
71449-091
Denver Solutions, LLC dba Leiters Health
2024-2
BEVACIZUMAB
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
25 mg/1 mL
71449-091-22
Bevacizumab
HUMAN COMPOUNDED DRUG
71449-091
Denver Solutions, LLC dba Leiters Health
2024-2
BEVACIZUMAB
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
25 mg/1 mL
71449-091-90
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