NDC 71335-3151 – Amitriptyline Hydrochloride

Amitriptyline Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3151

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212654
Marketed since
November 1, 2025
Listing expires
December 31, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-3151-1100 TABLET in 1 BOTTLE (71335-3151-1)Jun 29, 2026
71335-3151-230 TABLET in 1 BOTTLE (71335-3151-2)Jun 29, 2026
71335-3151-360 TABLET in 1 BOTTLE (71335-3151-3)Jun 29, 2026
71335-3151-490 TABLET in 1 BOTTLE (71335-3151-4)Jun 29, 2026
71335-3151-520 TABLET in 1 BOTTLE (71335-3151-5)Jun 29, 2026
71335-3151-628 TABLET in 1 BOTTLE (71335-3151-6)Jun 29, 2026
71335-3151-756 TABLET in 1 BOTTLE (71335-3151-7)Jun 29, 2026
71335-3151-8180 TABLET in 1 BOTTLE (71335-3151-8)Jun 29, 2026

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