Olanzapine

Product NDC
50090-2693
11-digit product format
500902693
Labeler code
50090
Product ID
50090-2693_0bb0477a-ceef-4cb7-9db1-0aed4ceaebfc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Olanzapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA076000
Marketing category
ANDA
Marketing start
2011-10-24
Marketing end
0000-00-00
Substance
OLANZAPINE
Active strength
10 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-2693-02020-01-31C16284748780-19d75b9d0-ae58-f424-e053-dadaa90a57ce757d0a64-6d77-43c1-bba2-5f533389d08d

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2693-0EA - Each50090-269303fd83ab-4588-448f-9b67-a91148d6d36f12019-04-11