mirtazapine

Generic: mirtazapine

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mirtazapine
Generic Name mirtazapine
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

mirtazapine 15 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2140
Product ID 50090-2140_a6586ed3-0ef9-44a9-b32d-9232dd5f964e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076921
Listing Expiration 2027-12-31
Marketing Start 2009-08-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902140
Hyphenated Format 50090-2140

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 ANDA076921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-2140-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-2140-1)
source: ndc

Packages (2)

Ingredients (1)

mirtazapine (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a6586ed3-0ef9-44a9-b32d-9232dd5f964e", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725", "314111"], "spl_set_id": ["67e753ad-9919-416b-9e8f-aab0fa808066"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2140-0)", "package_ndc": "50090-2140-0", "marketing_start_date": "20151019"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-2140-1)", "package_ndc": "50090-2140-1", "marketing_start_date": "20151019"}], "brand_name": "Mirtazapine", "product_id": "50090-2140_a6586ed3-0ef9-44a9-b32d-9232dd5f964e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50090-2140", "generic_name": "Mirtazapine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20090817", "listing_expiration_date": "20271231"}