liletta
Generic: levonorgestrel
Labeler: allergan, inc.Drug Facts
Product Profile
Brand Name
liletta
Generic Name
levonorgestrel
Labeler
allergan, inc.
Dosage Form
INTRAUTERINE DEVICE
Routes
Active Ingredients
levonorgestrel 52 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0023-5858
Product ID
0023-5858_2bd36b89-e6f6-4da1-97c4-3516f2a06b73
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA206229
Listing Expiration
2026-12-31
Marketing Start
2016-05-31
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00235858
Hyphenated Format
0023-5858
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
liletta (source: ndc)
Generic Name
levonorgestrel (source: ndc)
Application Number
NDA206229 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 52 mg/1
Packaging
- 1 TRAY in 1 CARTON (0023-5858-01) / 1 INTRAUTERINE DEVICE in 1 TRAY
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAUTERINE"], "spl_id": "2bd36b89-e6f6-4da1-97c4-3516f2a06b73", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "unii": ["5W7SIA7YZW"], "rxcui": ["1605252", "1605257"], "spl_set_id": ["aaf0eb2a-f88a-4f26-a445-0fd30176c326"], "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": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TRAY in 1 CARTON (0023-5858-01) / 1 INTRAUTERINE DEVICE in 1 TRAY", "package_ndc": "0023-5858-01", "marketing_start_date": "20160531"}], "brand_name": "LILETTA", "product_id": "0023-5858_2bd36b89-e6f6-4da1-97c4-3516f2a06b73", "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": "0023-5858", "generic_name": "Levonorgestrel", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LILETTA", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "52 mg/1"}], "application_number": "NDA206229", "marketing_category": "NDA", "marketing_start_date": "20160531", "listing_expiration_date": "20261231"}