Emcyt - 0013-0132-02 - (estramustine phosphate sodium)

Alphabetical Index


Drug Information of Emcyt

Product NDC: 0013-0132
Proprietary Name: Emcyt
Non Proprietary Name: estramustine phosphate sodium
Active Ingredient(s): 140    mg/1 & nbsp;   estramustine phosphate sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Emcyt

Product NDC: 0013-0132
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018045
Marketing Category: NDA
Start Marketing Date: 19920101

Package Information of Emcyt

Package NDC: 0013-0132-02
Package Description: 100 CAPSULE in 1 BOTTLE (0013-0132-02)

NDC Information of Emcyt

NDC Code 0013-0132-02
Proprietary Name Emcyt
Package Description 100 CAPSULE in 1 BOTTLE (0013-0132-02)
Product NDC 0013-0132
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estramustine phosphate sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19920101
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name ESTRAMUSTINE PHOSPHATE SODIUM
Strength Number 140
Strength Unit mg/1
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC],Estradiol [Chemical/Ingredient],Nitrogen Mustard Compounds [Chemical/Ingredient]

Complete Information of Emcyt


General Information