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LEVONORGESTREL AND ETHINYL ESTRADIOL
LEVONORGESTREL AND ETHINYL ESTRADIOL - 0378-6550-56 - (ethinyl estradiol and levonorgestrel)
Drug Information of LEVONORGESTREL AND ETHINYL ESTRADIOL
| Product NDC: | 0378-6550 |
| Proprietary Name: | LEVONORGESTREL AND ETHINYL ESTRADIOL |
| Non Proprietary Name: | ethinyl estradiol and levonorgestrel |
| Active Ingredient(s): | & nbsp; ethinyl estradiol and levonorgestrel |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVONORGESTREL AND ETHINYL ESTRADIOL
| Product NDC: | 0378-6550 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091663 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130101 |
Package Information of LEVONORGESTREL AND ETHINYL ESTRADIOL
| Package NDC: | 0378-6550-56 |
| Package Description: | 6 POUCH in 1 CARTON (0378-6550-56) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Information of LEVONORGESTREL AND ETHINYL ESTRADIOL
| NDC Code | 0378-6550-56 |
| Proprietary Name | LEVONORGESTREL AND ETHINYL ESTRADIOL |
| Package Description | 6 POUCH in 1 CARTON (0378-6550-56) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0378-6550 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ethinyl estradiol and levonorgestrel |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130101 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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