50419-423 : Mirena 52 mg Intrauterine Intrauterine Device
| NDC: | 50419-423 |
| Labeler: | Bayer Healthcare Pharmaceuticals Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Mirena |
| Dosage Form: | Intrauterine Intrauterine Device |
| Application #: | NDA021225 |
| Rev. Date: |
NDC Package Codes:
- 50419-423-01: 1 INTRAUTERINE DEVICE IN 1 CARTON (50419‑423‑01)
- 50419-423-08: 1 INTRAUTERINE DEVICE IN 1 CARTON (50419‑423‑08)
Active Ingredients:
- Levonorgestrel
Dosage Strength:
- 52 mg
Pharmaceutical Classes:
- Inhibit Ovum Fertilization [PE]
- Progesterone Congeners [CS]
- Progestin [EPC]
- Progestin-containing Intrauterine Device [EPC]
Related Products:
Based on records with the same trade name.- 50419-421 Mirena 52 mg/1 Intrauterine Intrauterine Device by Bayer Healthcare Pharmaceuticals Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.