amitriptyline hydrochloride

Generic: amitriptyline hydrochloride

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

amitriptyline hydrochloride 150 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1230
Product ID 70710-1230_5160111f-8889-4057-aa2a-519eccd14a5e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210086
Listing Expiration 2026-12-31
Marketing Start 2017-12-26

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101230
Hyphenated Format 70710-1230

Supplemental Identifiers

RxCUI
856762 856773 856783 856834 856845 856853
UPC
0370710122911 0370710122713
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 ANDA210086 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1230-0)
  • 100 TABLET, FILM COATED in 1 BOTTLE (70710-1230-1)
source: ndc

Packages (2)

70710-1230-0 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1230-0) 70710-1230-1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1230-1)

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": "5160111f-8889-4057-aa2a-519eccd14a5e", "openfda": {"upc": ["0370710122911", "0370710122713"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["73669354-babc-4687-a4fe-ad0fc1f863ba"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70710-1230-0)", "package_ndc": "70710-1230-0", "marketing_start_date": "20171226"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1230-1)", "package_ndc": "70710-1230-1", "marketing_start_date": "20171226"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70710-1230_5160111f-8889-4057-aa2a-519eccd14a5e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70710-1230", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20171226", "listing_expiration_date": "20261231"}