Package 50268-645-15

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50268-645-15
Digits Only 5026864515
Product NDC 50268-645
Product ID 50268-645_48ec761b-a7bc-59ef-e063-6294a90a579b
Description

50 BLISTER PACK in 1 BOX (50268-645-15) / 1 TABLET in 1 BLISTER PACK (50268-645-11)

Marketing

Marketing Status
Marketed Since 2018-07-09
Brand oxycodone and acetaminophen
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

Oxycodone and Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48ec761b-a7bc-59ef-e063-6294a90a579b", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["7055acd5-1cbb-397e-e053-2a91aa0a3852"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-645-15)  / 1 TABLET in 1 BLISTER PACK (50268-645-11)", "package_ndc": "50268-645-15", "marketing_start_date": "20180709"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "50268-645_48ec761b-a7bc-59ef-e063-6294a90a579b", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "50268-645", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA040778", "marketing_category": "ANDA", "marketing_start_date": "20180709", "listing_expiration_date": "20271231"}