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LEVONEST
LEVONEST - 34908-620-51 - (levonorgestrel and ethinyl estradiol)
Drug Information of LEVONEST
| Product NDC: | 34908-620 |
| Proprietary Name: | LEVONEST |
| 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 LEVONEST
| Product NDC: | 34908-620 |
| Labeler Name: | Novast Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090719 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110331 |
Package Information of LEVONEST
| Package NDC: | 34908-620-51 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (34908-620-51) > 1 KIT in 1 BLISTER PACK |
NDC Information of LEVONEST
| NDC Code | 34908-620-51 |
| Proprietary Name | LEVONEST |
| Package Description | 1 BLISTER PACK in 1 CARTON (34908-620-51) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 34908-620 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levonorgestrel and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20110331 |
| Marketing Category Name | ANDA |
| Labeler Name | Novast Laboratories, Ltd. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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