Package 68071-2368-6

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2368-6
Digits Only 6807123686
Product NDC 68071-2368
Product ID 68071-2368_4b455e52-2501-d55a-e063-6294a90a7ba6
Description

6 TABLET in 1 BOTTLE (68071-2368-6)

Marketing

Marketing Status
Marketed Since 2021-03-16
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": "4b455e52-2501-d55a-e063-6294a90a7ba6", "openfda": {"upc": ["0368071236866"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["bdade691-3687-3308-e053-2995a90ad6ed"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-2368-6)", "package_ndc": "68071-2368-6", "marketing_start_date": "20210316"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "68071-2368_4b455e52-2501-d55a-e063-6294a90a7ba6", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-2368", "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": "ANDA202160", "marketing_category": "ANDA", "marketing_start_date": "20120712", "listing_expiration_date": "20271231"}