amitriptyline hydrochloride

Generic: amitriptyline hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amitriptyline hydrochloride
Generic Name amitriptyline hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amitriptyline hydrochloride 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6179
Product ID 50090-6179_252c626f-1abb-4bd4-880b-504beb9ae6c7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214548
Listing Expiration 2026-12-31
Marketing Start 2021-05-26

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906179
Hyphenated Format 50090-6179

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 (50090-6179-0)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-6179-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6179-6)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-6179-7)
source: ndc

Packages (4)

50090-6179-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-6179-0) 50090-6179-1 100 TABLET, FILM COATED in 1 BOTTLE (50090-6179-1) 50090-6179-6 90 TABLET, FILM COATED in 1 BOTTLE (50090-6179-6) 50090-6179-7 60 TABLET, FILM COATED in 1 BOTTLE (50090-6179-7)

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": "252c626f-1abb-4bd4-880b-504beb9ae6c7", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["00d11130-c9ae-4258-9746-9763bc5deb84"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6179-0)", "package_ndc": "50090-6179-0", "marketing_start_date": "20221020"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-6179-1)", "package_ndc": "50090-6179-1", "marketing_start_date": "20221020"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6179-6)", "package_ndc": "50090-6179-6", "marketing_start_date": "20221020"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6179-7)", "package_ndc": "50090-6179-7", "marketing_start_date": "20231221"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-6179_252c626f-1abb-4bd4-880b-504beb9ae6c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-6179", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20210526", "listing_expiration_date": "20261231"}