NDC 72578-182 – Doxepin

Doxepin Hydrochloride 6 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72578-182

Product details

Brand name
Doxepin
Generic name
Doxepin
Labeler
Viona Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202761
Marketed since
June 30, 2024
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Doxepin →

Package NDC codes (6)

Package NDCDescriptionSince
72578-182-01100 TABLET in 1 BOTTLE (72578-182-01)Jun 30, 2024
72578-182-05500 TABLET in 1 BOTTLE (72578-182-05)Jun 30, 2024
72578-182-0630 TABLET in 1 BOTTLE (72578-182-06)Jun 30, 2024
72578-182-101000 TABLET in 1 BOTTLE (72578-182-10)Jun 30, 2024
72578-182-1690 TABLET in 1 BOTTLE (72578-182-16)Jun 30, 2024
72578-182-7710 BLISTER PACK in 1 CARTON (72578-182-77) / 10 TABLET in 1 BLISTER PACKJun 30, 2024

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