naltrexone hydrochloride
Generic: naltrexone hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
naltrexone hydrochloride
Generic Name
naltrexone hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
naltrexone hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2062
Product ID
71335-2062_ab44332a-6f04-4f07-8209-e472206d5707
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090356
Listing Expiration
2026-12-31
Marketing Start
2012-02-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352062
Hyphenated Format
71335-2062
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
naltrexone hydrochloride (source: ndc)
Generic Name
naltrexone hydrochloride (source: ndc)
Application Number
ANDA090356 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)
- 45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)
Packages (6)
71335-2062-1
30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)
71335-2062-2
90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)
71335-2062-3
60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)
71335-2062-4
45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)
71335-2062-5
120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)
71335-2062-6
15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ab44332a-6f04-4f07-8209-e472206d5707", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["f9807ec0-3504-4c66-8efe-ea25f84c782b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)", "package_ndc": "71335-2062-1", "marketing_start_date": "20220321"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)", "package_ndc": "71335-2062-2", "marketing_start_date": "20220321"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)", "package_ndc": "71335-2062-3", "marketing_start_date": "20220321"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)", "package_ndc": "71335-2062-4", "marketing_start_date": "20220321"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)", "package_ndc": "71335-2062-5", "marketing_start_date": "20220321"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)", "package_ndc": "71335-2062-6", "marketing_start_date": "20220321"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "71335-2062_ab44332a-6f04-4f07-8209-e472206d5707", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-2062", "generic_name": "NALTREXONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALTREXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090356", "marketing_category": "ANDA", "marketing_start_date": "20120229", "listing_expiration_date": "20261231"}