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Nortrel
Nortrel - 0555-9009-42 - (Norethindrone and Ethinyl Estradiol)
Drug Information of Nortrel
| Product NDC: | 0555-9009 |
| Proprietary Name: | Nortrel |
| Non Proprietary Name: | Norethindrone and Ethinyl Estradiol |
| Active Ingredient(s): | .035; 1 mg/1; mg/1 & nbsp; Norethindrone and Ethinyl Estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nortrel
| Product NDC: | 0555-9009 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072693 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010613 |
Package Information of Nortrel
| Package NDC: | 0555-9009-42 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (0555-9009-42) > 21 TABLET in 1 BLISTER PACK |
NDC Information of Nortrel
| NDC Code | 0555-9009-42 |
| Proprietary Name | Nortrel |
| Package Description | 3 BLISTER PACK in 1 CARTON (0555-9009-42) > 21 TABLET in 1 BLISTER PACK |
| Product NDC | 0555-9009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone and Ethinyl Estradiol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010613 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE |
| Strength Number | .035; 1 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
