Mirtazapine

Product NDC
80425-0305
11-digit product format
804250305
Labeler code
80425
Product ID
80425-0305_2a9ba8f4-6cee-e827-e063-6394a90a0300
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mirtazapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA076921
Marketing category
ANDA
Marketing start
2023-04-07
Substance
MIRTAZAPINE
Active strength
15 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA Listing Details

Product ID
80425-0305_2a9ba8f4-6cee-e827-e063-6394a90a0300
SPL ID
2a9ba8f4-6cee-e827-e063-6394a90a0300
Product type
HUMAN PRESCRIPTION DRUG
Finished product
Yes
Brand name base
Mirtazapine
Generic name
Mirtazapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Marketing start
2023-04-07
Marketing category
ANDA
Application number
ANDA076921
Listing expiration
2026-12-31

openFDA Active Ingredients

IngredientStrength
MIRTAZAPINE15 mg/1

openFDA Harmonized Identifiers

FieldValues
UniiA051Q2099Q
Rxcui311725
Spl Set Idf8c383c1-d1b3-ceaa-e053-6294a90a6053
Manufacturer NameAdvanced Rx Pharmacy of Tennessee, LLC

openFDA Package Details

Package NDCDescriptionMarketing startSample
80425-0305-130 TABLET, FILM COATED in 1 BOTTLE (80425-0305-1)2023-04-07No
80425-0305-260 TABLET, FILM COATED in 1 BOTTLE (80425-0305-2)2023-04-07No
80425-0305-390 TABLET, FILM COATED in 1 BOTTLE (80425-0305-3)2023-04-07No

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
A051Q2099QMIRTAZAPINE85650-52-8MIRTAZAPINE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
80425-0305-18042503050130 TABLET, FILM COATED in 1 BOTTLE (80425-0305-1) 2023-04-07NoNoHistorical
80425-0305-28042503050260 TABLET, FILM COATED in 1 BOTTLE (80425-0305-2) 2023-04-07NoNoHistorical
80425-0305-38042503050390 TABLET, FILM COATED in 1 BOTTLE (80425-0305-3) 2023-04-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Mirtazapine HCL TabletsAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL2