amitriptyline hydrochloride

Generic: amitriptyline hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amitriptyline hydrochloride
Generic Name amitriptyline hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amitriptyline hydrochloride 10 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3621
Product ID 70518-3621_3f18ad0d-ede1-76d9-e063-6394a90a1ef5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214548
Listing Expiration 2026-12-31
Marketing Start 2023-01-25

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183621
Hyphenated Format 70518-3621

Supplemental Identifiers

RxCUI
856783
UNII
26LUD4JO9K

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name amitriptyline hydrochloride (source: ndc)
Generic Name amitriptyline hydrochloride (source: ndc)
Application Number ANDA214548 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-1)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3621-2)
source: ndc

Packages (3)

70518-3621-0 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-0) 70518-3621-1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-1) 70518-3621-2 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3621-2)

Ingredients (1)

amitriptyline hydrochloride (10 mg/1)

Linked Drug Pages (1)

Amitriptyline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f18ad0d-ede1-76d9-e063-6394a90a1ef5", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["abf6a3f5-0df9-4b23-995d-63b973ef80c1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-0)", "package_ndc": "70518-3621-0", "marketing_start_date": "20230125"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-1)", "package_ndc": "70518-3621-1", "marketing_start_date": "20230128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3621-2)", "package_ndc": "70518-3621-2", "marketing_start_date": "20230505"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-3621_3f18ad0d-ede1-76d9-e063-6394a90a1ef5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3621", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230125", "listing_expiration_date": "20261231"}