Mirtazapine

Product NDC
0093-7207
11-digit product format
000937207
Labeler code
0093
Product ID
0093-7207_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
30 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
0093-7207-19EA - Each0093-72074dd6f6ae-8eb0-465e-8188-4c06449e2b0a12012-07-24
0093-7207-56EA - Each0093-72073f702b26-32eb-4d26-988a-d2b4a43b8f8912012-07-24
0093-7207-93EA - Each0093-7207f0ae555f-72f2-4a0e-86b7-7d61f9bd93a612012-07-24

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