mirtazapine

Generic: mirtazapine

Labeler: mckesson corporation dba sky packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mirtazapine
Generic Name mirtazapine
Labeler mckesson corporation dba sky packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

mirtazapine 30 mg/1

Manufacturer
McKesson Corporation dba SKY Packaging

Identifiers & Regulatory

Product NDC 63739-099
Product ID 63739-099_2bb25f3c-7005-6710-e063-6294a90a022c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077666
Marketing Start 2007-08-22
Marketing End 2027-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739099
Hyphenated Format 63739-099

Supplemental Identifiers

RxCUI
311725 314111
UNII
A051Q2099Q

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 mirtazapine (source: ndc)
Generic Name mirtazapine (source: ndc)
Application Number ANDA077666 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BOX (63739-099-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

63739-099-10 10 BLISTER PACK in 1 BOX (63739-099-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

mirtazapine (30 mg/1)

Linked Drug Pages (1)

Mirtazapine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2bb25f3c-7005-6710-e063-6294a90a022c", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725", "314111"], "spl_set_id": ["40c95daa-bbd5-48d9-97e4-c87f2c1f0fa5"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX (63739-099-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "63739-099-10", "marketing_end_date": "20270331", "marketing_start_date": "20191115"}], "brand_name": "Mirtazapine", "product_id": "63739-099_2bb25f3c-7005-6710-e063-6294a90a022c", "dosage_form": "TABLET, FILM COATED", "product_ndc": "63739-099", "generic_name": "Mirtazapine", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA077666", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20070822"}