Package 72865-202-05
Brand: hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophenPackage Facts
Identity
Package NDC
72865-202-05
Digits Only
7286520205
Product NDC
72865-202
Description
500 TABLET in 1 BOTTLE (72865-202-05)
Marketing
Marketing Status
Brand
hydrocodone bitartrate and acetaminophen
Generic
hydrocodone bitartrate and acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4533550e-d20a-4329-b5ab-fb7542ce0be9", "openfda": {"upc": ["0372865204054", "0372865201015", "0372865203057", "0372865203019", "0372865202050", "0372865204016", "0372865202012"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005", "857391"], "spl_set_id": ["b9f61b9c-d3f9-47e3-94a3-b5228f96f927"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-202-01)", "package_ndc": "72865-202-01", "marketing_start_date": "20200227"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-202-05)", "package_ndc": "72865-202-05", "marketing_start_date": "20200227"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "72865-202_4533550e-d20a-4329-b5ab-fb7542ce0be9", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72865-202", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA211487", "marketing_category": "ANDA", "marketing_start_date": "20200227", "listing_expiration_date": "20261231"}