Package 53746-145-01

Brand: hydrocodone bitartrate and ibuprofen

Generic: hydrocodone bitartrate and ibuprofen
NDC Package

Package Facts

Identity

Package NDC 53746-145-01
Digits Only 5374614501
Product NDC 53746-145
Description

100 TABLET in 1 BOTTLE (53746-145-01)

Marketing

Marketing Status
Marketed Since 2010-02-18
Brand hydrocodone bitartrate and ibuprofen
Generic hydrocodone bitartrate and ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e109d65b-643b-4c2e-80ad-30c7b3e9c160", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0353746117014", "0353746145017", "0353746116017", "0353746146014"], "unii": ["WK2XYI10QM", "NO70W886KK"], "rxcui": ["858770", "858778", "858798", "859315"], "spl_set_id": ["abc33718-4e88-43ea-9ffa-2b04ffc812ef"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53746-145-01)", "package_ndc": "53746-145-01", "marketing_start_date": "20100218"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (53746-145-05)", "package_ndc": "53746-145-05", "marketing_start_date": "20100218"}], "brand_name": "Hydrocodone Bitartrate and Ibuprofen", "product_id": "53746-145_e109d65b-643b-4c2e-80ad-30c7b3e9c160", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "53746-145", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Ibuprofen", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Ibuprofen", "active_ingredients": [{"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA076642", "marketing_category": "ANDA", "marketing_start_date": "20100218", "listing_expiration_date": "20261231"}