Crinone - 52544-284-02 - (progesterone)

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Drug Information of Crinone

Product NDC: 52544-284
Proprietary Name: Crinone
Non Proprietary Name: progesterone
Active Ingredient(s): 90    mg/1.125g & nbsp;   progesterone
Administration Route(s): VAGINAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Crinone

Product NDC: 52544-284
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020701
Marketing Category: NDA
Start Marketing Date: 19970513

Package Information of Crinone

Package NDC: 52544-284-02
Package Description: 2 APPLICATOR in 1 CARTON (52544-284-02) > 1.125 g in 1 APPLICATOR

NDC Information of Crinone

NDC Code 52544-284-02
Proprietary Name Crinone
Package Description 2 APPLICATOR in 1 CARTON (52544-284-02) > 1.125 g in 1 APPLICATOR
Product NDC 52544-284
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name progesterone
Dosage Form Name GEL
Route Name VAGINAL
Start Marketing Date 19970513
Marketing Category Name NDA
Labeler Name Watson Pharma, Inc.
Substance Name PROGESTERONE
Strength Number 90
Strength Unit mg/1.125g
Pharmaceutical Classes Progesterone [Chemical/Ingredient],Progesterone [EPC]

Complete Information of Crinone


General Information