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Beyaz
Beyaz - 50419-407-00 - (Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium)
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: | 50419-407-00 |
| Package Description: | 90 BLISTER PACK in 1 PACKAGE (50419-407-00) > 1 KIT in 1 BLISTER PACK |
NDC Information of Beyaz
| NDC Code | 50419-407-00 |
| Proprietary Name | Beyaz |
| Package Description | 90 BLISTER PACK in 1 PACKAGE (50419-407-00) > 1 KIT in 1 BLISTER PACK |
| 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 |
