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FALMINA
FALMINA - 16714-359-02 - (Levonorgestrel and Ethinyl Estradiol)
Drug Information of FALMINA
| Product NDC: | 16714-359 |
| Proprietary Name: | FALMINA |
| Non Proprietary Name: | Levonorgestrel and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Levonorgestrel and Ethinyl Estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FALMINA
| Product NDC: | 16714-359 |
| Labeler Name: | Northstar Rx LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090721 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120701 |
Package Information of FALMINA
| Package NDC: | 16714-359-02 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (16714-359-02) > 1 KIT in 1 BLISTER PACK |
NDC Information of FALMINA
| NDC Code | 16714-359-02 |
| Proprietary Name | FALMINA |
| Package Description | 1 BLISTER PACK in 1 CARTON (16714-359-02) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 16714-359 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20120701 |
| Marketing Category Name | ANDA |
| Labeler Name | Northstar Rx LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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