liletta

Generic: levonorgestrel

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name liletta
Generic Name levonorgestrel
Labeler allergan, inc.
Dosage Form INTRAUTERINE DEVICE
Routes
INTRAUTERINE
Active Ingredients

levonorgestrel 52 mg/1

Manufacturer
Allergan, Inc.

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)
progestin [epc] progestin-containing intrauterine system [epc]
Chemical Structure
progesterone congeners [cs]
Physiologic Effect
inhibit ovum fertilization [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00235858
Hyphenated Format 0023-5858

Supplemental Identifiers

RxCUI
1605252 1605257
UNII
5W7SIA7YZW
NUI
N0000175830 M0447349 N0000175602 N0000175832

Packaging Origin

Original Packager
true

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
INTRAUTERINE
source: ndc

Resolved Composition

Strengths
  • 52 mg/1
source: ndc
Packaging
  • 1 TRAY in 1 CARTON (0023-5858-01) / 1 INTRAUTERINE DEVICE in 1 TRAY
source: ndc

Packages (1)

Ingredients (1)

levonorgestrel (52 mg/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"}