mirena
Generic: levonorgestrel
Labeler: bayer healthcare pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
mirena
Generic Name
levonorgestrel
Labeler
bayer healthcare pharmaceuticals inc.
Dosage Form
INTRAUTERINE DEVICE
Routes
Active Ingredients
levonorgestrel 52 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50419-423
Product ID
50419-423_ab3e1924-b102-48c1-8188-a089524e9dd0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021225
Listing Expiration
2026-12-31
Marketing Start
2009-10-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50419423
Hyphenated Format
50419-423
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
mirena (source: ndc)
Generic Name
levonorgestrel (source: ndc)
Application Number
NDA021225 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 52 mg/1
Packaging
- 1 INTRAUTERINE DEVICE in 1 CARTON (50419-423-01)
- 1 INTRAUTERINE DEVICE in 1 CARTON (50419-423-08)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAUTERINE"], "spl_id": "ab3e1924-b102-48c1-8188-a089524e9dd0", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "unii": ["5W7SIA7YZW"], "rxcui": ["804156", "807283"], "spl_set_id": ["dcbd6aa2-b3fa-479a-a676-56ea742962fc"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_pe": ["Inhibit Ovum Fertilization [PE]"], "pharm_class_epc": ["Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "manufacturer_name": ["Bayer HealthCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INTRAUTERINE DEVICE in 1 CARTON (50419-423-01)", "package_ndc": "50419-423-01", "marketing_start_date": "20140530"}, {"sample": false, "description": "1 INTRAUTERINE DEVICE in 1 CARTON (50419-423-08)", "package_ndc": "50419-423-08", "marketing_start_date": "20161208"}], "brand_name": "Mirena", "product_id": "50419-423_ab3e1924-b102-48c1-8188-a089524e9dd0", "dosage_form": "INTRAUTERINE DEVICE", "pharm_class": ["Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "product_ndc": "50419-423", "generic_name": "Levonorgestrel", "labeler_name": "Bayer HealthCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirena", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "52 mg/1"}], "application_number": "NDA021225", "marketing_category": "NDA", "marketing_start_date": "20091001", "listing_expiration_date": "20261231"}