Natazia - 50419-409-03 - (estradiol valerate and estradiol valerate/dienogest)

Alphabetical Index


Drug Information of Natazia

Product NDC: 50419-409
Proprietary Name: Natazia
Non Proprietary Name: estradiol valerate and estradiol valerate/dienogest
Active Ingredient(s):    & nbsp;   estradiol valerate and estradiol valerate/dienogest
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Natazia

Product NDC: 50419-409
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022252
Marketing Category: NDA
Start Marketing Date: 20100506

Package Information of Natazia

Package NDC: 50419-409-03
Package Description: 3 BLISTER PACK in 1 PACKAGE (50419-409-03) > 1 KIT in 1 BLISTER PACK (50419-409-01)

NDC Information of Natazia

NDC Code 50419-409-03
Proprietary Name Natazia
Package Description 3 BLISTER PACK in 1 PACKAGE (50419-409-03) > 1 KIT in 1 BLISTER PACK (50419-409-01)
Product NDC 50419-409
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estradiol valerate and estradiol valerate/dienogest
Dosage Form Name KIT
Route Name
Start Marketing Date 20100506
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Natazia


General Information