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Acetylcysteine - 55154-5731-5 - (Acetylcysteine)

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Drug Information of Acetylcysteine

Product NDC: 55154-5731
Proprietary Name: Acetylcysteine
Non Proprietary Name: Acetylcysteine
Active Ingredient(s): 200    mg/mL & nbsp;   Acetylcysteine
Administration Route(s): ORAL; RESPIRATORY (INHALATION)
Dosage Form(s): INHALANT
Coding System: National Drug Codes(NDC)

Labeler Information of Acetylcysteine

Product NDC: 55154-5731
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110506

Package Information of Acetylcysteine

Package NDC: 55154-5731-5
Package Description: 5 VIAL in 1 BAG (55154-5731-5) > 4 mL in 1 VIAL

NDC Information of Acetylcysteine

NDC Code 55154-5731-5
Proprietary Name Acetylcysteine
Package Description 5 VIAL in 1 BAG (55154-5731-5) > 4 mL in 1 VIAL
Product NDC 55154-5731
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetylcysteine
Dosage Form Name INHALANT
Route Name ORAL; RESPIRATORY (INHALATION)
Start Marketing Date 20110506
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Cardinal Health
Substance Name ACETYLCYSTEINE
Strength Number 200
Strength Unit mg/mL
Pharmaceutical Classes Antidote [EPC],Antidote for Acetaminophen Overdose [EPC],Decreased Respiratory Secretion Viscosity [PE],Increased Glutathione Concentration [PE],Mucolytic [EPC],Reduction Activity [MoA]

Complete Information of Acetylcysteine


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