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Dehydrated Alcohol - 0517-8571-10 - (Dehydrated Alcohol)

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Drug Information of Dehydrated Alcohol

Product NDC: 0517-8571
Proprietary Name: Dehydrated Alcohol
Non Proprietary Name: Dehydrated Alcohol
Active Ingredient(s): .98    mL/mL & nbsp;   Dehydrated Alcohol
Administration Route(s): INTRASPINAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dehydrated Alcohol

Product NDC: 0517-8571
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900930

Package Information of Dehydrated Alcohol

Package NDC: 0517-8571-10
Package Description: 10 AMPULE in 1 BOX (0517-8571-10) > 1 mL in 1 AMPULE

NDC Information of Dehydrated Alcohol

NDC Code 0517-8571-10
Proprietary Name Dehydrated Alcohol
Package Description 10 AMPULE in 1 BOX (0517-8571-10) > 1 mL in 1 AMPULE
Product NDC 0517-8571
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dehydrated Alcohol
Dosage Form Name INJECTION, SOLUTION
Route Name INTRASPINAL
Start Marketing Date 19900930
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name American Regent, Inc.
Substance Name ALCOHOL
Strength Number .98
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Dehydrated Alcohol


General Information