Package 13811-703-10

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13811-703-10
Digits Only 1381170310
Product NDC 13811-703
Product ID 13811-703_e22a1e07-ff84-4ef1-b154-804b49dcd52f
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-703-10)

Marketing

Marketing Status
Marketed Since 2016-09-15
Brand hydromorphone hydrochloride
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydromorphone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e22a1e07-ff84-4ef1-b154-804b49dcd52f", "openfda": {"upc": ["0313811701104", "0313811703108", "0313811704105", "0313811702101"], "unii": ["L960UP2KRW"], "rxcui": ["902729", "902736", "902741", "1306898", "2706360"], "spl_set_id": ["8bb81796-6990-40e9-bee4-1f292f91ae99"], "manufacturer_name": ["Trigen Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-703-10)", "package_ndc": "13811-703-10", "marketing_start_date": "20160915"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "13811-703_e22a1e07-ff84-4ef1-b154-804b49dcd52f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "13811-703", "dea_schedule": "CII", "generic_name": "Hydromorphone Hydrochloride", "labeler_name": "Trigen Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "16 mg/1"}], "application_number": "ANDA205629", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}