| Product NDC: | 42254-287 |
| Proprietary Name: | Necon 0.5/35 |
| Non Proprietary Name: | Norethindrone and Ethinyl Estradiol Tablets |
| Active Ingredient(s): | & nbsp; Norethindrone and Ethinyl Estradiol Tablets |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42254-287 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070686 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870129 |
| Package NDC: | 42254-287-28 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (42254-287-28) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 42254-287-28 |
| Proprietary Name | Necon 0.5/35 |
| Package Description | 1 BLISTER PACK in 1 CARTON (42254-287-28) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 42254-287 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone and Ethinyl Estradiol Tablets |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19870129 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |