mirtazapine

Product NDC
0185-0020
11-digit product format
001850020
Labeler code
0185
Product ID
0185-0020_d423d909-f428-4514-9814-e0a6b94de27a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
mirtazapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Eon Labs, Inc.
Application
ANDA076219
Marketing category
ANDA
Marketing start
2003-06-19
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0185-0020-10EA - Each0185-0020597a1063-c03f-45cc-95d3-d416b8d926da12012-07-24
0185-0020-30EA - Each0185-0020d59252b6-4202-4e82-b1d8-729fa0cb319712012-07-24

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311725mirtazapine 15 MG Oral TabletPSN5a1ce60e-977b-1801-e053-2a91aa0adb5e1
311725mirtazapine 15 MG Oral TabletSCD5a1ce60e-977b-1801-e053-2a91aa0adb5e1