mirtazapine

Generic: mirtazapine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mirtazapine
Generic Name mirtazapine
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

mirtazapine 30 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0964
Product ID 71335-0964_956bdf1e-236a-4ebe-ac0c-f035adf4b4bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076921
Listing Expiration 2026-12-31
Marketing Start 2004-10-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350964
Hyphenated Format 71335-0964

Supplemental Identifiers

RxCUI
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
  • 30 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0964-1)
  • 56 TABLET, FILM COATED in 1 BOTTLE (71335-0964-2)
  • 15 TABLET, FILM COATED in 1 BOTTLE (71335-0964-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0964-4)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0964-5)
  • 28 TABLET, FILM COATED in 1 BOTTLE (71335-0964-6)
  • 45 TABLET, FILM COATED in 1 BOTTLE (71335-0964-7)
source: ndc

Packages (7)

71335-0964-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0964-1) 71335-0964-2 56 TABLET, FILM COATED in 1 BOTTLE (71335-0964-2) 71335-0964-3 15 TABLET, FILM COATED in 1 BOTTLE (71335-0964-3) 71335-0964-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-0964-4) 71335-0964-5 60 TABLET, FILM COATED in 1 BOTTLE (71335-0964-5) 71335-0964-6 28 TABLET, FILM COATED in 1 BOTTLE (71335-0964-6) 71335-0964-7 45 TABLET, FILM COATED in 1 BOTTLE (71335-0964-7)

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": "956bdf1e-236a-4ebe-ac0c-f035adf4b4bd", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["314111"], "spl_set_id": ["1fb26f9b-b075-471d-8cc3-fa39246ec2e4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0964-1)", "package_ndc": "71335-0964-1", "marketing_start_date": "20181008"}, {"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (71335-0964-2)", "package_ndc": "71335-0964-2", "marketing_start_date": "20240409"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-0964-3)", "package_ndc": "71335-0964-3", "marketing_start_date": "20200810"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0964-4)", "package_ndc": "71335-0964-4", "marketing_start_date": "20190808"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0964-5)", "package_ndc": "71335-0964-5", "marketing_start_date": "20240409"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-0964-6)", "package_ndc": "71335-0964-6", "marketing_start_date": "20240409"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71335-0964-7)", "package_ndc": "71335-0964-7", "marketing_start_date": "20240409"}], "brand_name": "Mirtazapine", "product_id": "71335-0964_956bdf1e-236a-4ebe-ac0c-f035adf4b4bd", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71335-0964", "generic_name": "Mirtazapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20041022", "listing_expiration_date": "20261231"}