myalept

Generic: metreleptin

Labeler: chiesi usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name myalept
Generic Name metreleptin
Labeler chiesi usa, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
SUBCUTANEOUS
Active Ingredients

metreleptin 11.3 mg/2.2mL

Manufacturer
Chiesi USA, Inc.

Identifiers & Regulatory

Product NDC 10122-210
Product ID 10122-210_8b236f4c-7654-49fe-bca9-ab947b72a1fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA125390
Listing Expiration 2026-12-31
Marketing Start 2015-03-05

Pharmacologic Class

Established (EPC)
leptin analog [epc]
Chemical Structure
analogs/derivatives [chemical/ingredient] leptin [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10122210
Hyphenated Format 10122-210

Supplemental Identifiers

RxCUI
1491629 1491634
UPC
0310122210028
UNII
TL60C27RLH
NUI
N0000190854 N0000175452 N0000170333

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 myalept (source: ndc)
Generic Name metreleptin (source: ndc)
Application Number BLA125390 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 11.3 mg/2.2mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (10122-210-02) / 2.2 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (1)

metreleptin (11.3 mg/2.2mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "8b236f4c-7654-49fe-bca9-ab947b72a1fd", "openfda": {"nui": ["N0000190854", "N0000175452", "N0000170333"], "upc": ["0310122210028"], "unii": ["TL60C27RLH"], "rxcui": ["1491629", "1491634"], "spl_set_id": ["d3b50bbd-140b-425c-b5ec-d4682aad62bc"], "pharm_class_cs": ["Analogs/Derivatives [Chemical/Ingredient]", "Leptin [Chemical/Ingredient]"], "pharm_class_epc": ["Leptin Analog [EPC]"], "manufacturer_name": ["Chiesi USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (10122-210-02)  / 2.2 mL in 1 VIAL, GLASS", "package_ndc": "10122-210-02", "marketing_start_date": "20150305"}], "brand_name": "Myalept", "product_id": "10122-210_8b236f4c-7654-49fe-bca9-ab947b72a1fd", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Analogs/Derivatives [Chemical/Ingredient]", "Leptin Analog [EPC]", "Leptin [Chemical/Ingredient]"], "product_ndc": "10122-210", "generic_name": "metreleptin", "labeler_name": "Chiesi USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Myalept", "active_ingredients": [{"name": "METRELEPTIN", "strength": "11.3 mg/2.2mL"}], "application_number": "BLA125390", "marketing_category": "BLA", "marketing_start_date": "20150305", "listing_expiration_date": "20261231"}