Package 64380-262-01

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64380-262-01
Digits Only 6438026201
Product NDC 64380-262
Product ID 64380-262_226ed432-8e6c-4de6-840c-55c6379f9064
Description

100 TABLET in 1 BOTTLE, PLASTIC (64380-262-01)

Marketing

Marketing Status
Marketed Since 2024-09-10
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": "226ed432-8e6c-4de6-840c-55c6379f9064", "openfda": {"upc": ["0364380262015", "0364380260011", "0364380259015", "0364380261018", "0364380263012"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["f3116ebf-d72c-4e98-aa50-006be4770c86"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (64380-262-01)", "package_ndc": "64380-262-01", "marketing_start_date": "20240910"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "64380-262_226ed432-8e6c-4de6-840c-55c6379f9064", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "64380-262", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20240910", "listing_expiration_date": "20271231"}