Package 13107-004-99
Brand: hydrocodone bitartrate and ibuprofen
Generic: hydrocodone bitartrate and ibuprofenPackage Facts
Identity
Package NDC
13107-004-99
Digits Only
1310700499
Product NDC
13107-004
Description
1000 TABLET, FILM COATED in 1 BOTTLE (13107-004-99)
Marketing
Marketing Status
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": "ef408ee9-6806-423f-9998-53d81cc71b94", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0313107004018"], "unii": ["NO70W886KK", "WK2XYI10QM"], "rxcui": ["858798"], "spl_set_id": ["470df63a-5c0f-42df-9023-a330a901153e"], "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": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (13107-004-01)", "package_ndc": "13107-004-01", "marketing_start_date": "20160602"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13107-004-05)", "package_ndc": "13107-004-05", "marketing_start_date": "20160602"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (13107-004-11)", "package_ndc": "13107-004-11", "marketing_start_date": "20160602"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (13107-004-99)", "package_ndc": "13107-004-99", "marketing_start_date": "20160602"}], "brand_name": "Hydrocodone Bitartrate and Ibuprofen", "product_id": "13107-004_ef408ee9-6806-423f-9998-53d81cc71b94", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "13107-004", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Ibuprofen", "labeler_name": "Aurolife Pharma, 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": "ANDA204575", "marketing_category": "ANDA", "marketing_start_date": "20160602", "listing_expiration_date": "20261231"}