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Ascorbic Acid - 0389-0486-50 - (Ascorbic Acid)

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Drug Information of Ascorbic Acid

Product NDC: 0389-0486
Proprietary Name: Ascorbic Acid
Non Proprietary Name: Ascorbic Acid
Active Ingredient(s): 500    mg/mL & nbsp;   Ascorbic Acid
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ascorbic Acid

Product NDC: 0389-0486
Labeler Name: The Torrance Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19990601

Package Information of Ascorbic Acid

Package NDC: 0389-0486-50
Package Description: 50 VIAL, DISPENSING in 1 CARTON (0389-0486-50) > 50 mL in 1 VIAL, DISPENSING

NDC Information of Ascorbic Acid

NDC Code 0389-0486-50
Proprietary Name Ascorbic Acid
Package Description 50 VIAL, DISPENSING in 1 CARTON (0389-0486-50) > 50 mL in 1 VIAL, DISPENSING
Product NDC 0389-0486
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ascorbic Acid
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19990601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name The Torrance Company
Substance Name ASCORBIC ACID
Strength Number 500
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Ascorbic Acid


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