Package 17856-0101-1

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 17856-0101-1
Digits Only 1785601011
Product NDC 17856-0101
Product ID 17856-0101_3892e59b-daa3-17b8-e063-6394a90a00f5
Description

100 POUCH in 1 BOX, UNIT-DOSE (17856-0101-1) / 1 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2021-05-12
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (1)

Mirtazapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3892e59b-daa3-17b8-e063-6394a90a00f5", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["e6e5cbf7-a958-4ef8-abcc-a7491edb9520"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (17856-0101-1)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "17856-0101-1", "marketing_start_date": "20210512"}], "brand_name": "Mirtazapine", "product_id": "17856-0101_3892e59b-daa3-17b8-e063-6394a90a00f5", "dosage_form": "TABLET, FILM COATED", "product_ndc": "17856-0101", "generic_name": "Mirtazapine", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20090817", "listing_expiration_date": "20261231"}