amitriptyline hydrochloride
Generic: amitriptyline hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
amitriptyline hydrochloride
Generic Name
amitriptyline hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
amitriptyline hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1256
Product ID
71335-1256_0f092778-43f5-15d0-e063-6394a90a1215
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089399
Listing Expiration
2026-12-31
Marketing Start
1987-07-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351256
Hyphenated Format
71335-1256
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
ANDA089399 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1256-1)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1256-2)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1256-3)
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1256-4)
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1256-5)
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-1256-6)
- 56 TABLET, FILM COATED in 1 BOTTLE (71335-1256-7)
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-1256-8)
Packages (8)
71335-1256-1
100 TABLET, FILM COATED in 1 BOTTLE (71335-1256-1)
71335-1256-2
30 TABLET, FILM COATED in 1 BOTTLE (71335-1256-2)
71335-1256-3
60 TABLET, FILM COATED in 1 BOTTLE (71335-1256-3)
71335-1256-4
90 TABLET, FILM COATED in 1 BOTTLE (71335-1256-4)
71335-1256-5
20 TABLET, FILM COATED in 1 BOTTLE (71335-1256-5)
71335-1256-6
28 TABLET, FILM COATED in 1 BOTTLE (71335-1256-6)
71335-1256-7
56 TABLET, FILM COATED in 1 BOTTLE (71335-1256-7)
71335-1256-8
180 TABLET, FILM COATED in 1 BOTTLE (71335-1256-8)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0f092778-43f5-15d0-e063-6394a90a1215", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["dcdeb999-412e-475f-a21d-2e0ac42d136e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1256-1)", "package_ndc": "71335-1256-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1256-2)", "package_ndc": "71335-1256-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1256-3)", "package_ndc": "71335-1256-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1256-4)", "package_ndc": "71335-1256-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1256-5)", "package_ndc": "71335-1256-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-1256-6)", "package_ndc": "71335-1256-6", "marketing_start_date": "20220209"}, {"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (71335-1256-7)", "package_ndc": "71335-1256-7", "marketing_start_date": "20220209"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-1256-8)", "package_ndc": "71335-1256-8", "marketing_start_date": "20220209"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "71335-1256_0f092778-43f5-15d0-e063-6394a90a1215", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71335-1256", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA089399", "marketing_category": "ANDA", "marketing_start_date": "19870714", "listing_expiration_date": "20261231"}