Package 47335-326-18
Brand: naltrexone hydrochloride
Generic: naltrexone hydrochloridePackage Facts
Identity
Package NDC
47335-326-18
Digits Only
4733532618
Product NDC
47335-326
Description
1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)
Marketing
Marketing Status
Brand
naltrexone hydrochloride
Generic
naltrexone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0c2b60a-dc96-483b-933e-2fed58b64372", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["0f30f885-d0cd-4fa6-a8e0-142f08a56792"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-326-08)", "package_ndc": "47335-326-08", "marketing_start_date": "20120229"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)", "package_ndc": "47335-326-18", "marketing_start_date": "20120229"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-326-83)", "package_ndc": "47335-326-83", "marketing_start_date": "20120229"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-326-88)", "package_ndc": "47335-326-88", "marketing_start_date": "20120229"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "47335-326_b0c2b60a-dc96-483b-933e-2fed58b64372", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "47335-326", "generic_name": "NALTREXONE HYDROCHLORIDE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "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"}