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Lidocaine HCl and Hydrocortisone Acetate - 0168-0479-14 - (Lidocaine Hydrochloride and Hydrocortisone Acetate)

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Drug Information of Lidocaine HCl and Hydrocortisone Acetate

Product NDC: 0168-0479
Proprietary Name: Lidocaine HCl and Hydrocortisone Acetate
Non Proprietary Name: Lidocaine Hydrochloride and Hydrocortisone Acetate
Active Ingredient(s): 5; 30    mg/g; mg/g & nbsp;   Lidocaine Hydrochloride and Hydrocortisone Acetate
Administration Route(s): RECTAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine HCl and Hydrocortisone Acetate

Product NDC: 0168-0479
Labeler Name: E. Fougera & Co. A division of Nycomed US Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100119

Package Information of Lidocaine HCl and Hydrocortisone Acetate

Package NDC: 0168-0479-14
Package Description: 7 g in 1 TUBE (0168-0479-14)

NDC Information of Lidocaine HCl and Hydrocortisone Acetate

NDC Code 0168-0479-14
Proprietary Name Lidocaine HCl and Hydrocortisone Acetate
Package Description 7 g in 1 TUBE (0168-0479-14)
Product NDC 0168-0479
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride and Hydrocortisone Acetate
Dosage Form Name CREAM
Route Name RECTAL
Start Marketing Date 20100119
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name E. Fougera & Co. A division of Nycomed US Inc.
Substance Name HYDROCORTISONE ACETATE; LIDOCAINE HYDROCHLORIDE
Strength Number 5; 30
Strength Unit mg/g; mg/g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Lidocaine HCl and Hydrocortisone Acetate


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