Mirtazapine

Product NDC
45865-382
11-digit product format
458650382
Labeler code
45865
Product ID
45865-382_9701f4c5-12e4-1b12-e053-2a95a90a4dd1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mirtazapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Medsource Pharmaceuticals
Application
ANDA076921
Marketing category
ANDA
Marketing start
2009-08-17
Marketing end
0000-00-00
Substance
MIRTAZAPINE
Active strength
15 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1ca5a24a-fafa-8fc8-52ac-b403ff18faa5Product name320240216
a733d273-402b-1005-9891-1ac1a9c63703Product name220170724

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
45865-382-30Mirtazapine30 in 1 BOTTLETABLET, FILM COATED302
45865-382-60Mirtazapine60 in 1 BOTTLETABLET, FILM COATED602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
45865-382MIRTAZAPINE TABLET, FILM COATED [MEDSOURCE PHARMACEUTICALS]2Legacy NDC, 2 package rows20191111_1d6161e3-2e4e-5446-e054-00144ff8d46c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311725mirtazapine 15 MG Oral TabletPSN1d6161e3-2e4e-5446-e054-00144ff8d46c2
311725mirtazapine 15 MG Oral TabletSCD1d6161e3-2e4e-5446-e054-00144ff8d46c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
45865-382-304586503823030 TABLET, FILM COATED in 1 BOTTLE (45865-382-30) 2015-08-190000-00-00NoNoCurrent
45865-382-604586503826060 TABLET, FILM COATED in 1 BOTTLE (45865-382-60) 2015-08-190000-00-00NoNoCurrent