Mirtazapine

Product NDC
0093-7206
11-digit product format
000937206
Labeler code
0093
Product ID
0093-7206_7064d29d-da21-4a64-9451-a211af369381
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mirtazapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA076119
Marketing category
ANDA
Marketing start
2003-01-29
Marketing end
2020-02-29
Substance
MIRTAZAPINE
Active strength
15 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
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
0093-7206-19EA - Each0093-720662d1474c-fb59-493a-98b6-5f456b896b1912012-07-24
0093-7206-56EA - Each0093-7206904612d5-eb6a-4f1f-94b9-256cdc5c1b5c12012-07-24
0093-7206-93EA - Each0093-7206b08ac3ae-1651-4638-b840-96cf6593bc5712012-07-24

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311725mirtazapine 15 MG Oral TabletPSN1d4ca80a-5360-49d0-a3aa-b551b5b0de0221
314111mirtazapine 30 MG Oral TabletPSN1d4ca80a-5360-49d0-a3aa-b551b5b0de0221
311725mirtazapine 15 MG Oral TabletSCD1d4ca80a-5360-49d0-a3aa-b551b5b0de0221
314111mirtazapine 30 MG Oral TabletSCD1d4ca80a-5360-49d0-a3aa-b551b5b0de0221