amitriptyline hydrochloride

Generic: amitriptyline hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amitriptyline hydrochloride
Generic Name amitriptyline hydrochloride
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amitriptyline hydrochloride 25 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-433
Product ID 60687-433_44706732-5523-8018-e063-6294a90a9cc7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210086
Listing Expiration 2026-12-31
Marketing Start 2019-08-15

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687433
Hyphenated Format 60687-433

Supplemental Identifiers

RxCUI
856834 856845
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 ANDA210086 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-433-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-433-11)
source: ndc

Packages (1)

60687-433-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-433-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-433-11)

Ingredients (1)

amitriptyline hydrochloride (25 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": "44706732-5523-8018-e063-6294a90a9cc7", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834", "856845"], "spl_set_id": ["98cc0bf3-ae5b-47cc-992f-9157fed7c3f4"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-433-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-433-11)", "package_ndc": "60687-433-01", "marketing_start_date": "20190815"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "60687-433_44706732-5523-8018-e063-6294a90a9cc7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60687-433", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20190815", "listing_expiration_date": "20261231"}