amitriptyline hydrochloride

Generic: amitriptyline hydrochloride

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amitriptyline hydrochloride
Generic Name amitriptyline hydrochloride
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amitriptyline hydrochloride 150 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-424
Product ID 29300-424_3f6bcdb5-c8ad-45c0-b43f-2dbea8980376
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 29300424
Hyphenated Format 29300-424

Supplemental Identifiers

RxCUI
856762 856773 856783 856834 856845 856853
UPC
0329300420012
UNII
26LUD4JO9K

Packaging Origin

Original Packager
true

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
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (29300-424-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (29300-424-05)
source: ndc

Packages (2)

29300-424-01 100 TABLET, FILM COATED in 1 BOTTLE (29300-424-01) 29300-424-05 500 TABLET, FILM COATED in 1 BOTTLE (29300-424-05)

Ingredients (1)

amitriptyline hydrochloride (150 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": "3f6bcdb5-c8ad-45c0-b43f-2dbea8980376", "openfda": {"upc": ["0329300420012"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["9c6e0e05-b579-4fae-b768-e1a664c39bb8"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (29300-424-01)", "package_ndc": "29300-424-01", "marketing_start_date": "20210526"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (29300-424-05)", "package_ndc": "29300-424-05", "marketing_start_date": "20210526"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "29300-424_3f6bcdb5-c8ad-45c0-b43f-2dbea8980376", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "29300-424", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}