Doxepin Hydrochloride

Product NDC
63629-7852
11-digit product format
636297852
Labeler code
63629
Product ID
63629-7852_005f0da3-20f2-40ae-9907-d05ff47b2ce5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxepin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA071422
Marketing category
ANDA
Marketing start
2017-09-01
Marketing end
0000-00-00
Substance
DOXEPIN HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63629-7852-12020-10-12C16284748780-19d75b9d0-9913-f424-e053-dadaa90a57ce15b86f88-41cd-4f23-b02f-c20e1cb5c5a5
63629-7852-12020-01-31C16284748780-19d75b9d0-9913-f424-e053-dadaa90a57ce15b86f88-41cd-4f23-b02f-c20e1cb5c5a5