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Lidocaine HCl - Hydrocortisone Acetate - 59088-819-20 - (Lidocaine HCl and Hydrocortisone Acetate)

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Drug Information of Lidocaine HCl - Hydrocortisone Acetate

Product NDC: 59088-819
Proprietary Name: Lidocaine HCl - Hydrocortisone Acetate
Non Proprietary Name: Lidocaine HCl and Hydrocortisone Acetate
Active Ingredient(s): 5; 30    mg/g; mg/g & nbsp;   Lidocaine HCl and Hydrocortisone Acetate
Administration Route(s): RECTAL; TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine HCl - Hydrocortisone Acetate

Product NDC: 59088-819
Labeler Name: PureTek Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110701

Package Information of Lidocaine HCl - Hydrocortisone Acetate

Package NDC: 59088-819-20
Package Description: 20 TUBE in 1 KIT (59088-819-20) > 7 g in 1 TUBE (59088-819-01)

NDC Information of Lidocaine HCl - Hydrocortisone Acetate

NDC Code 59088-819-20
Proprietary Name Lidocaine HCl - Hydrocortisone Acetate
Package Description 20 TUBE in 1 KIT (59088-819-20) > 7 g in 1 TUBE (59088-819-01)
Product NDC 59088-819
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine HCl and Hydrocortisone Acetate
Dosage Form Name CREAM
Route Name RECTAL; TOPICAL
Start Marketing Date 20110701
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name PureTek Corporation
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 - Hydrocortisone Acetate


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