Mibelas 24 Fe is a Kit in the Human Prescription Drug category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is .
| Product ID | 68180-911_40cb8d07-1594-4ea0-8ae4-fbc2fb882380 |
| NDC | 68180-911 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Mibelas 24 Fe |
| Generic Name | Norethindrone Acetate, Ethinyl Estradiol And Ferrous Fumarate |
| Dosage Form | Kit |
| Marketing Start Date | 2017-01-25 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA206287 |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2020-03-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA206287 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2020-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA206287 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2020-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA206287 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2017-01-25 |
| Marketing End Date | 2021-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA206287 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2017-01-25 |
| Marketing End Date | 2021-10-31 |
| SPL SET ID: | 3f82d240-1d26-409e-87cd-10c1d5a511c2 |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |