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Analpram HC - 0496-0799-33 - (hydrocortisone acetate and pramoxine hydrochloride)

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Drug Information of Analpram HC

Product NDC: 0496-0799
Proprietary Name: Analpram HC
Non Proprietary Name: hydrocortisone acetate and pramoxine hydrochloride
Active Ingredient(s): 25; 10    mg/g; mg/g & nbsp;   hydrocortisone acetate and pramoxine hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Analpram HC

Product NDC: 0496-0799
Labeler Name: Ferndale Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20091015

Package Information of Analpram HC

Package NDC: 0496-0799-33
Package Description: 4 g in 1 TUBE, WITH APPLICATOR (0496-0799-33)

NDC Information of Analpram HC

NDC Code 0496-0799-33
Proprietary Name Analpram HC
Package Description 4 g in 1 TUBE, WITH APPLICATOR (0496-0799-33)
Product NDC 0496-0799
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocortisone acetate and pramoxine hydrochloride
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20091015
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Ferndale Laboratories, Inc.
Substance Name HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Strength Number 25; 10
Strength Unit mg/g; mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Analpram HC


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