Podofilox - 0591-3204-13 - (Podofilox)

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Drug Information of Podofilox

Product NDC: 0591-3204
Proprietary Name: Podofilox
Non Proprietary Name: Podofilox
Active Ingredient(s): 5    mg/mL & nbsp;   Podofilox
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Podofilox

Product NDC: 0591-3204
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019795
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19901213

Package Information of Podofilox

Package NDC: 0591-3204-13
Package Description: 3.5 mL in 1 BOTTLE, GLASS (0591-3204-13)

NDC Information of Podofilox

NDC Code 0591-3204-13
Proprietary Name Podofilox
Package Description 3.5 mL in 1 BOTTLE, GLASS (0591-3204-13)
Product NDC 0591-3204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Podofilox
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 19901213
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Watson Laboratories, Inc.
Substance Name PODOFILOX
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Decreased Mitosis [PE]

Complete Information of Podofilox


General Information