Beyaz - 50419-407-75 - (Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium)

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Drug Information of Beyaz

Product NDC: 50419-407
Proprietary Name: Beyaz
Non Proprietary Name: Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Active Ingredient(s):    & nbsp;   Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Beyaz

Product NDC: 50419-407
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022532
Marketing Category: NDA
Start Marketing Date: 20101007

Package Information of Beyaz

Package NDC: 50419-407-75
Package Description: 12 PACKAGE in 1 CARTON (50419-407-75) > 5 BLISTER PACK in 1 PACKAGE > 1 KIT in 1 BLISTER PACK (50419-407-71)

NDC Information of Beyaz

NDC Code 50419-407-75
Proprietary Name Beyaz
Package Description 12 PACKAGE in 1 CARTON (50419-407-75) > 5 BLISTER PACK in 1 PACKAGE > 1 KIT in 1 BLISTER PACK (50419-407-71)
Product NDC 50419-407
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Dosage Form Name KIT
Route Name
Start Marketing Date 20101007
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Beyaz


General Information