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ACD Solution Modified - 51808-201-01 - (ACD Solution Modified)

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Drug Information of ACD Solution Modified

Product NDC: 51808-201
Proprietary Name: ACD Solution Modified
Non Proprietary Name: ACD Solution Modified
Active Ingredient(s): 8    mg/mL & nbsp;   ACD Solution Modified
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ACD Solution Modified

Product NDC: 51808-201
Labeler Name: AnazaoHealth Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120523

Package Information of ACD Solution Modified

Package NDC: 51808-201-01
Package Description: 10 mL in 1 VIAL (51808-201-01)

NDC Information of ACD Solution Modified

NDC Code 51808-201-01
Proprietary Name ACD Solution Modified
Package Description 10 mL in 1 VIAL (51808-201-01)
Product NDC 51808-201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ACD Solution Modified
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120523
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name AnazaoHealth Corporation
Substance Name ANHYDROUS CITRIC ACID
Strength Number 8
Strength Unit mg/mL
Pharmaceutical Classes Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]

Complete Information of ACD Solution Modified


General Information