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 | |
Pharmaceutical Classes |