Package 71863-216-04

Brand: increlex

Generic: mecasermin
NDC Package

Package Facts

Identity

Package NDC 71863-216-04
Digits Only 7186321604
Product NDC 71863-216
Product ID 71863-216_3b2a53e0-f43e-4f64-e063-6294a90af024
Description

1 VIAL, MULTI-DOSE in 1 CARTON (71863-216-04) / 4 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2025-04-16
Brand increlex
Generic mecasermin
Sample Package No

Linked Drug Pages (1)

Increlex ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "3b2a53e0-f43e-4f64-e063-6294a90af024", "openfda": {"unii": ["7GR9I2683O"], "rxcui": ["604806", "615882"], "spl_set_id": ["d5b2b0e1-c523-468d-9a0b-4ae4e4a8dbce"], "manufacturer_name": ["Eton Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (71863-216-04)  / 4 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71863-216-04", "marketing_start_date": "20250416"}], "brand_name": "Increlex", "product_id": "71863-216_3b2a53e0-f43e-4f64-e063-6294a90af024", "dosage_form": "INJECTION", "product_ndc": "71863-216", "generic_name": "Mecasermin", "labeler_name": "Eton Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Increlex", "active_ingredients": [{"name": "MECASERMIN", "strength": "40 mg/4mL"}], "application_number": "BLA021839", "marketing_category": "BLA", "marketing_start_date": "20250416", "listing_expiration_date": "20261231"}