Home
>
National Drug Code (NDC)
>
LOESTRIN 1/20
LOESTRIN 1/20 - 51285-079-97 - (norethindrone acetate and ethinyl estradiol)
Drug Information of LOESTRIN 1/20
| Product NDC: | 51285-079 |
| Proprietary Name: | LOESTRIN 1/20 |
| Non Proprietary Name: | norethindrone acetate and ethinyl estradiol |
| Active Ingredient(s): | 20; 1 ug/1; mg/1 & nbsp; norethindrone acetate and ethinyl estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LOESTRIN 1/20
| Product NDC: | 51285-079 |
| Labeler Name: | Teva Women's Health, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076380 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081001 |
Package Information of LOESTRIN 1/20
| Package NDC: | 51285-079-97 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (51285-079-97) > 21 TABLET in 1 BLISTER PACK |
NDC Information of LOESTRIN 1/20
| NDC Code | 51285-079-97 |
| Proprietary Name | LOESTRIN 1/20 |
| Package Description | 5 BLISTER PACK in 1 CARTON (51285-079-97) > 21 TABLET in 1 BLISTER PACK |
| Product NDC | 51285-079 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone acetate and ethinyl estradiol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081001 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Women's Health, Inc |
| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
| Strength Number | 20; 1 |
| Strength Unit | ug/1; mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
