DOXEPIN HYDROCHLORIDE

Product NDC
71335-1704
11-digit product format
713351704
Labeler code
71335
Product ID
71335-1704_c5b2b33b-6391-4dfd-9411-fffa3f02870a
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
10 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1704DOXEPIN HYDROCHLORIDE CAPSULE [BRYANT RANCH PREPACK]101Legacy NDC20201016_c5b2b33b-6391-4dfd-9411-fffa3f02870a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1704-17133517040130 CAPSULE in 1 BOTTLE (71335-1704-1) 30 capsule2020-09-100000-00-00NoNoCurrent
71335-1704-27133517040260 CAPSULE in 1 BOTTLE (71335-1704-2) 60 capsule2020-10-150000-00-00NoNoCurrent
71335-1704-37133517040318 CAPSULE in 1 BOTTLE (71335-1704-3) 18 capsule2020-10-150000-00-00NoNoCurrent
71335-1704-47133517040490 CAPSULE in 1 BOTTLE (71335-1704-4) 90 capsule2020-10-150000-00-00NoNoCurrent
71335-1704-571335170405180 CAPSULE in 1 BOTTLE (71335-1704-5) 180 capsule2020-10-150000-00-00NoNoCurrent