NDC 71335-3007 – Amitriptyline Hydrochloride

Amitriptyline Hydrochloride 10 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-3007

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA212654
Marketed since
May 20, 2024
Listing expires
December 31, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-3007-0100 TABLET, COATED in 1 BOTTLE (71335-3007-0)Feb 4, 2026
71335-3007-130 TABLET, COATED in 1 BOTTLE (71335-3007-1)Feb 4, 2026
71335-3007-215 TABLET, COATED in 1 BOTTLE (71335-3007-2)Feb 4, 2026
71335-3007-360 TABLET, COATED in 1 BOTTLE (71335-3007-3)Feb 4, 2026
71335-3007-490 TABLET, COATED in 1 BOTTLE (71335-3007-4)Feb 4, 2026
71335-3007-528 TABLET, COATED in 1 BOTTLE (71335-3007-5)Feb 4, 2026
71335-3007-6120 TABLET, COATED in 1 BOTTLE (71335-3007-6)Feb 4, 2026
71335-3007-750 TABLET, COATED in 1 BOTTLE (71335-3007-7)Feb 4, 2026
71335-3007-8180 TABLET, COATED in 1 BOTTLE (71335-3007-8)Feb 4, 2026
71335-3007-96 TABLET, COATED in 1 BOTTLE (71335-3007-9)Feb 4, 2026

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