Imipramine Hydrochloride

Product NDC
50090-0034
11-digit product format
500900034
Labeler code
50090
Product ID
50090-0034_72b9a3d9-9253-4833-88fd-1e49a7873e81
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Imipramine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA088262
Marketing category
ANDA
Marketing start
1983-10-21
Marketing end
0000-00-00
Substance
IMIPRAMINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-0034-02021-06-14C16284748780-19d75b9d1-1f0b-f424-e053-dadaa90a57ce484009c3-0609-400e-b4ce-e5120ad9b430
50090-0034-02020-01-31C16284748780-19d75b9d1-1f0b-f424-e053-dadaa90a57ce484009c3-0609-400e-b4ce-e5120ad9b430

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-0034-0EA - Each50090-0034661bef0e-fa49-465e-8f3b-2e098ac0ffa812018-08-13