Desipramine Hydrochloride

Product NDC: 0781-8218
11-digit product format: 007818218
Labeler code: 0781
Product ID: 0781-8218_83ae3fcf-2c05-4ee1-8e68-6649eda49344
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desipramine Hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Sandoz Inc
Application: ANDA072099
Marketing category: ANDA
Marketing start: 1988-05-24
Marketing end: 0000-00-00
Substance: DESIPRAMINE HYDROCHLORIDE
Active strength: 10 mg/1
Pharmacologic classes: Tricyclic Antidepressant [EPC]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
bda46dda-4ebd-3e63-0043-123c9d173af2	Product name	6	20220125

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0781-8218-01	EA - Each	0781-8218	d6d64df1-0430-448c-aaf3-6d556de60724	1	2018-11-06

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1099288	desipramine HCl 10 MG Oral Tablet	PSN	a7e6d256-7226-3334-e053-2995a90aa96d	1
1099288	desipramine hydrochloride 10 MG Oral Tablet	SCD	a7e6d256-7226-3334-e053-2995a90aa96d	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0781-8218-01	00781821801	100 TABLET, FILM COATED in 1 BOTTLE (0781-8218-01)	2018-09-19	0000-00-00	No	No	Current