Doxepin Hydrochloride

Product NDC
72162-2227
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxepin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA213474
Marketing category
ANDA
Substance
DOXEPIN HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2227-1100 CAPSULE in 1 BOTTLE (72162-2227-1) 2024-01-26NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Doxepin Hydrochloride Capsules, USP 10 mg, 25 mg, 50 mg, 75 mg and 100 mgBryant Ranch Prepack2024-01-26HUMAN PRESCRIPTION DRUG LABEL100