Home
>
National Drug Code (NDC)
>
Safyral
Safyral - 50419-403-75 - (Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium)
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 |
