Mirtazapine

Product NDC
33261-073
11-digit product format
332610073
Labeler code
33261
Product ID
33261-073_c25beec4-de6c-4516-a172-f7408248831a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mirtazapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
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
2019-12-31
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
33261-073-30Mirtazapine30 in 1 BOTTLE, PLASTICTABLET, FILM COATED301
33261-073-60Mirtazapine60 in 1 BOTTLE, PLASTICTABLET, FILM COATED601
33261-073-90Mirtazapine90 in 1 BOTTLE, PLASTICTABLET, FILM COATED901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33261-073MIRTAZAPINE TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]1Legacy NDC, 3 package rows20140128_20b2b378-f493-4f57-a5c1-54865d8c0183.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311725mirtazapine 15 MG Oral TabletPSN20b2b378-f493-4f57-a5c1-54865d8c01831
311725mirtazapine 15 MG Oral TabletSCD20b2b378-f493-4f57-a5c1-54865d8c01831

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
33261-073-303326100733030 in 1 BOTTLE, PLASTICHistorical
33261-073-603326100736060 in 1 BOTTLE, PLASTICHistorical
33261-073-903326100739090 in 1 BOTTLE, PLASTICHistorical