DOXEPIN HYDROCHLORIDE

Product NDC
71335-1770
11-digit product format
713351770
Labeler code
71335
Product ID
71335-1770_b36354a9-ad0c-4e76-88e5-28dbef7cb5c8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
DOXEPIN HYDROCHLORIDE
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA213063
Marketing category
ANDA
Marketing start
2020-07-01
Marketing end
0000-00-00
Substance
DOXEPIN HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1770DOXEPIN HYDROCHLORIDE CAPSULE [BRYANT RANCH PREPACK]100Legacy NDC20210421_c641035a-084f-4ffa-a005-e234a424965a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1770-17133517700130 CAPSULE in 1 BOTTLE (71335-1770-1) 30 capsule2021-03-110000-00-00NoNoCurrent
71335-1770-27133517700260 CAPSULE in 1 BOTTLE (71335-1770-2) 60 capsule2021-03-110000-00-00NoNoCurrent
71335-1770-37133517700328 CAPSULE in 1 BOTTLE (71335-1770-3) 28 capsule2021-03-110000-00-00NoNoCurrent
71335-1770-47133517700418 CAPSULE in 1 BOTTLE (71335-1770-4) 18 capsule2021-03-110000-00-00NoNoCurrent
71335-1770-57133517700590 CAPSULE in 1 BOTTLE (71335-1770-5) 90 capsule2021-03-110000-00-00NoNoCurrent