Doxepin Hydrochloride

Product NDC
63629-3221
11-digit product format
636293221
Labeler code
63629
Product ID
63629-3221_c42ed494-2d4d-424c-9663-fb51872a638e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
doxepin hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA070791
Marketing category
ANDA
Marketing start
1986-05-13
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-3221-1EA - Each63629-32217af4ac75-764e-46b4-b0e7-260453022a8a12013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-3221-16362932210130 CAPSULE in 1 BOTTLE (63629-3221-1) 30 capsule2006-07-130000-00-00NoNoCurrent
63629-3221-26362932210260 CAPSULE in 1 BOTTLE (63629-3221-2) 60 capsule2022-04-290000-00-00NoNoCurrent
63629-3221-36362932210318 CAPSULE in 1 BOTTLE (63629-3221-3) 18 capsule2022-04-290000-00-00NoNoCurrent
63629-3221-46362932210490 CAPSULE in 1 BOTTLE (63629-3221-4) 90 capsule2022-04-290000-00-00NoNoCurrent
63629-3221-563629322105180 CAPSULE in 1 BOTTLE (63629-3221-5) 180 capsule2022-04-290000-00-00NoNoCurrent