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Lidocaine Hydrochloride and Hydrocortisone Acetate - 13925-160-01 - (Lidocaine Hydrochloride and Hydrocortisone Acetate)

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Drug Information of Lidocaine Hydrochloride and Hydrocortisone Acetate

Product NDC: 13925-160
Proprietary Name: Lidocaine Hydrochloride 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): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride and Hydrocortisone Acetate

Product NDC: 13925-160
Labeler Name: Seton Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110617

Package Information of Lidocaine Hydrochloride and Hydrocortisone Acetate

Package NDC: 13925-160-01
Package Description: 1 TUBE in 1 CARTON (13925-160-01) > 28.35 g in 1 TUBE

NDC Information of Lidocaine Hydrochloride and Hydrocortisone Acetate

NDC Code 13925-160-01
Proprietary Name Lidocaine Hydrochloride and Hydrocortisone Acetate
Package Description 1 TUBE in 1 CARTON (13925-160-01) > 28.35 g in 1 TUBE
Product NDC 13925-160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride and Hydrocortisone Acetate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110617
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Seton Pharmaceuticals
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 Hydrochloride and Hydrocortisone Acetate


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