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
Routes
Active Ingredients
amitriptyline hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2374
Product ID
71335-2374_3a62a016-ae4b-4c92-aa9f-eb4f097e2c6c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217411
Listing Expiration
2026-12-31
Marketing Start
2023-06-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352374
Hyphenated Format
71335-2374
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
- 100 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-2374-1)
- 60 TABLET in 1 BOTTLE (71335-2374-2)
- 90 TABLET in 1 BOTTLE (71335-2374-3)
- 180 TABLET in 1 BOTTLE (71335-2374-4)
- 28 TABLET in 1 BOTTLE (71335-2374-5)
- 120 TABLET in 1 BOTTLE (71335-2374-6)
- 18 TABLET in 1 BOTTLE (71335-2374-7)
- 8 TABLET in 1 BOTTLE (71335-2374-8)
Packages (8)
71335-2374-1
30 TABLET in 1 BOTTLE (71335-2374-1)
71335-2374-2
60 TABLET in 1 BOTTLE (71335-2374-2)
71335-2374-3
90 TABLET in 1 BOTTLE (71335-2374-3)
71335-2374-4
180 TABLET in 1 BOTTLE (71335-2374-4)
71335-2374-5
28 TABLET in 1 BOTTLE (71335-2374-5)
71335-2374-6
120 TABLET in 1 BOTTLE (71335-2374-6)
71335-2374-7
18 TABLET in 1 BOTTLE (71335-2374-7)
71335-2374-8
8 TABLET in 1 BOTTLE (71335-2374-8)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a62a016-ae4b-4c92-aa9f-eb4f097e2c6c", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["c707a873-6b67-478f-aa3c-d206a59cbe6d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2374-1)", "package_ndc": "71335-2374-1", "marketing_start_date": "20240529"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2374-2)", "package_ndc": "71335-2374-2", "marketing_start_date": "20240529"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2374-3)", "package_ndc": "71335-2374-3", "marketing_start_date": "20240529"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2374-4)", "package_ndc": "71335-2374-4", "marketing_start_date": "20240529"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2374-5)", "package_ndc": "71335-2374-5", "marketing_start_date": "20240529"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2374-6)", "package_ndc": "71335-2374-6", "marketing_start_date": "20240529"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-2374-7)", "package_ndc": "71335-2374-7", "marketing_start_date": "20240529"}, {"sample": false, "description": "8 TABLET in 1 BOTTLE (71335-2374-8)", "package_ndc": "71335-2374-8", "marketing_start_date": "20240529"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "71335-2374_3a62a016-ae4b-4c92-aa9f-eb4f097e2c6c", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71335-2374", "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": "100 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}