| Product NDC: | 42254-242 |
| Proprietary Name: | Junel Fe 1.5/30 |
| Non Proprietary Name: | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
| Active Ingredient(s): | & nbsp; norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42254-242 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076064 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110121 |
| Package NDC: | 42254-242-28 |
| Package Description: | 1 KIT in 1 BLISTER PACK (42254-242-28) |
| NDC Code | 42254-242-28 |
| Proprietary Name | Junel Fe 1.5/30 |
| Package Description | 1 KIT in 1 BLISTER PACK (42254-242-28) |
| Product NDC | 42254-242 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110121 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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