Home
>
National Drug Code (NDC)
>
Junel Fe 1/20
Junel Fe 1/20 - 0555-9026-58 - (norethindrone acetate and ethinyl estradiol, and ferrous fumarate)
Drug Information of Junel Fe 1/20
| Product NDC: | 0555-9026 |
| Proprietary Name: | Junel Fe 1/20 |
| 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) |
Labeler Information of Junel Fe 1/20
| Product NDC: | 0555-9026 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076081 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030918 |
Package Information of Junel Fe 1/20
| Package NDC: | 0555-9026-58 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (0555-9026-58) > 1 KIT in 1 BLISTER PACK |
NDC Information of Junel Fe 1/20
| NDC Code | 0555-9026-58 |
| Proprietary Name | Junel Fe 1/20 |
| Package Description | 6 BLISTER PACK in 1 CARTON (0555-9026-58) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0555-9026 |
| 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 | 20030918 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
