Safyral - 50419-403-75 - (Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium)

Alphabetical Index


Drug Information of Safyral

Product NDC: 50419-403
Proprietary Name: Safyral
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 Safyral

Product NDC: 50419-403
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022574
Marketing Category: NDA
Start Marketing Date: 20120213

Package Information of Safyral

Package NDC: 50419-403-75
Package Description: 12 PACKAGE in 1 CARTON (50419-403-75) > 5 BLISTER PACK in 1 PACKAGE > 1 KIT in 1 BLISTER PACK (50419-403-71)

NDC Information of Safyral

NDC Code 50419-403-75
Proprietary Name Safyral
Package Description 12 PACKAGE in 1 CARTON (50419-403-75) > 5 BLISTER PACK in 1 PACKAGE > 1 KIT in 1 BLISTER PACK (50419-403-71)
Product NDC 50419-403
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 20120213
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Safyral


General Information