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
Routes
ORAL
Active Ingredients

mirtazapine 15 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0286
Product ID 71335-0286_7bcab2eb-126f-4e34-949a-a7002e06ed12
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076541
Listing Expiration 2026-12-31
Marketing Start 2004-04-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350286
Hyphenated Format 71335-0286

Supplemental Identifiers

RxCUI
311725
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 ANDA076541 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0286-1)
  • 60 TABLET in 1 BOTTLE (71335-0286-2)
  • 90 TABLET in 1 BOTTLE (71335-0286-3)
  • 120 TABLET in 1 BOTTLE (71335-0286-4)
  • 15 TABLET in 1 BOTTLE (71335-0286-5)
  • 180 TABLET in 1 BOTTLE (71335-0286-6)
  • 45 TABLET in 1 BOTTLE (71335-0286-7)
  • 21 TABLET in 1 BOTTLE (71335-0286-8)
source: ndc

Packages (8)

71335-0286-1 30 TABLET in 1 BOTTLE (71335-0286-1) 71335-0286-2 60 TABLET in 1 BOTTLE (71335-0286-2) 71335-0286-3 90 TABLET in 1 BOTTLE (71335-0286-3) 71335-0286-4 120 TABLET in 1 BOTTLE (71335-0286-4) 71335-0286-5 15 TABLET in 1 BOTTLE (71335-0286-5) 71335-0286-6 180 TABLET in 1 BOTTLE (71335-0286-6) 71335-0286-7 45 TABLET in 1 BOTTLE (71335-0286-7) 71335-0286-8 21 TABLET in 1 BOTTLE (71335-0286-8)

Ingredients (1)

mirtazapine (15 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": "7bcab2eb-126f-4e34-949a-a7002e06ed12", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["9f0f52e8-3318-4da2-b0d9-ea3d33bfe41e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0286-1)", "package_ndc": "71335-0286-1", "marketing_start_date": "20210909"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0286-2)", "package_ndc": "71335-0286-2", "marketing_start_date": "20211108"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0286-3)", "package_ndc": "71335-0286-3", "marketing_start_date": "20211227"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0286-4)", "package_ndc": "71335-0286-4", "marketing_start_date": "20211227"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-0286-5)", "package_ndc": "71335-0286-5", "marketing_start_date": "20211227"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0286-6)", "package_ndc": "71335-0286-6", "marketing_start_date": "20211227"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-0286-7)", "package_ndc": "71335-0286-7", "marketing_start_date": "20211227"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-0286-8)", "package_ndc": "71335-0286-8", "marketing_start_date": "20211227"}], "brand_name": "Mirtazapine", "product_id": "71335-0286_7bcab2eb-126f-4e34-949a-a7002e06ed12", "dosage_form": "TABLET", "product_ndc": "71335-0286", "generic_name": "Mirtazapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA076541", "marketing_category": "ANDA", "marketing_start_date": "20040422", "listing_expiration_date": "20261231"}