amitriptyline hydrochloride
Generic: amitriptyline hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
amitriptyline hydrochloride
Generic Name
amitriptyline hydrochloride
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
amitriptyline hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7410
Product ID
0904-7410_54771c13-f83b-4c28-b2ed-be967b14d388
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217411
Listing Expiration
2026-12-31
Marketing Start
2024-03-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047410
Hyphenated Format
0904-7410
Supplemental Identifiers
RxCUI
UNII
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
ANDA217411 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (0904-7410-61) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "54771c13-f83b-4c28-b2ed-be967b14d388", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834", "856845"], "spl_set_id": ["29ec1221-04d8-4b21-822e-2779fcaae62c"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7410-61) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7410-61", "marketing_start_date": "20240308"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "0904-7410_54771c13-f83b-4c28-b2ed-be967b14d388", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0904-7410", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20240308", "listing_expiration_date": "20261231"}