NDC 82804-957 – Imipramine Hydrochloride

Imipramine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-957

Product details

Brand name
Imipramine Hydrochloride
Generic name
Imipramine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040751
Marketed since
August 1, 2020
Listing expires
December 31, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Imipramine Hydrochloride →

Package NDC codes (7)

Package NDCDescriptionSince
82804-957-00100 TABLET in 1 BOTTLE (82804-957-00)Jan 12, 2026
82804-957-111000 TABLET in 1 BOTTLE (82804-957-11)Jan 12, 2026
82804-957-3030 TABLET in 1 BOTTLE (82804-957-30)Jan 12, 2026
82804-957-55500 TABLET in 1 BOTTLE (82804-957-55)Jan 12, 2026
82804-957-6060 TABLET in 1 BOTTLE (82804-957-60)Jan 12, 2026
82804-957-72120 TABLET in 1 BOTTLE (82804-957-72)Jan 12, 2026
82804-957-9090 TABLET in 1 BOTTLE (82804-957-90)Jan 12, 2026

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