NDC 62332-639 – Doxepin Hydrochloride

Doxepin Hydrochloride 75 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC62332-639

Product details

Brand name
Doxepin Hydrochloride
Generic name
Doxepin Hydrochloride
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA215076
Marketed since
April 23, 2021
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Doxepin hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
62332-639-31100 CAPSULE in 1 BOTTLE (62332-639-31)Apr 23, 2021
62332-639-911000 CAPSULE in 1 BOTTLE (62332-639-91)Apr 23, 2021

Recalls mentioning this NDC

Other Doxepin hydrochloride products