Desipramine Hydrochloride

Product NDC: 24724-068
11-digit product format: 247240068
Labeler code: 24724
Product ID: 24724-068_494d7b7e-4fdc-4d1a-8b7e-4a8b163b4ab0
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desipramine Hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: INDICUS PHARMA LLC
Application: ANDA207433
Marketing category: ANDA
Marketing start: 2016-08-01
Marketing end: 0000-00-00
Substance: DESIPRAMINE HYDROCHLORIDE
Active strength: 25 mg/1
Pharmacologic classes: Tricyclic Antidepressant [EPC]
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
24724-068-03	2020-01-31	C162847	48780-1	9d75b9d0-a55b-f424-e053-dadaa90a57ce	3bada7cf-8ca2-46e9-b7db-ff21b2af03f7
24724-068-50	2020-01-31	C162847	48780-1	9d75b9d0-a55b-f424-e053-dadaa90a57ce	3bada7cf-8ca2-46e9-b7db-ff21b2af03f7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
24724-068	DESIPRAMINE HYDROCHLORIDE TABLET [INDICUS PHARMA LLC]	4	Legacy NDC	20160801_3bada7cf-8ca2-46e9-b7db-ff21b2af03f7.zip