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Myzilra
Myzilra - 0603-7625-49 - (Levonorgestrel and Ethinyl Estradiol)
Drug Information of Myzilra
| Product NDC: | 0603-7625 |
| Proprietary Name: | Myzilra |
| Non Proprietary Name: | Levonorgestrel and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Levonorgestrel and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Myzilra
| Product NDC: | 0603-7625 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077502 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120112 |
Package Information of Myzilra
| Package NDC: | 0603-7625-49 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (0603-7625-49) > 1 KIT in 1 BLISTER PACK (0603-7625-01) |
NDC Information of Myzilra
| NDC Code | 0603-7625-49 |
| Proprietary Name | Myzilra |
| Package Description | 3 BLISTER PACK in 1 CARTON (0603-7625-49) > 1 KIT in 1 BLISTER PACK (0603-7625-01) |
| Product NDC | 0603-7625 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120112 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
