Doxepin Hydrochloride

Product NDC
71335-2452
11-digit product format
713352452
Labeler code
71335
Product ID
71335-2452_34b2b0a0-565f-46cf-bd8c-c0b6902f3c8f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxepin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA215113
Marketing category
ANDA
Marketing start
2022-06-27
Substance
DOXEPIN HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
3U9A0FE9N5DOXEPIN HYDROCHLORIDE1229-29-4DOXEPIN HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2452-17133524520130 CAPSULE in 1 BOTTLE, PLASTIC (71335-2452-1) 30 capsule2024-08-20NoNoHistorical
71335-2452-27133524520260 CAPSULE in 1 BOTTLE, PLASTIC (71335-2452-2) 60 capsule2024-08-20NoNoHistorical
71335-2452-37133524520318 CAPSULE in 1 BOTTLE, PLASTIC (71335-2452-3) 18 capsule2024-08-20NoNoHistorical
71335-2452-47133524520490 CAPSULE in 1 BOTTLE, PLASTIC (71335-2452-4) 90 capsule2024-08-20NoNoHistorical
71335-2452-571335245205180 CAPSULE in 1 BOTTLE, PLASTIC (71335-2452-5) 180 capsule2024-08-20NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Doxepin Hydrochloride Capsules, USPBryant Ranch Prepack2024-08-20HUMAN PRESCRIPTION DRUG LABEL1