Package 68071-2899-4

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2899-4
Digits Only 6807128994
Product NDC 68071-2899
Product ID 68071-2899_217adc8e-b886-1fdb-e063-6294a90a26fa
Description

4 TABLET in 1 BOTTLE, PLASTIC (68071-2899-4)

Marketing

Marketing Status
Marketed Since 2022-12-08
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "217adc8e-b886-1fdb-e063-6294a90a26fa", "openfda": {"upc": ["0368071289961"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["ef58f422-682e-6896-e053-2a95a90a1f2d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (68071-2899-4)", "package_ndc": "68071-2899-4", "marketing_start_date": "20221208"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (68071-2899-6)", "package_ndc": "68071-2899-6", "marketing_start_date": "20221208"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "68071-2899_217adc8e-b886-1fdb-e063-6294a90a26fa", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-2899", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}