Package 13107-261-58
Brand: oxycodone hydrochloride oral solution
Generic: oxycodone hydrochloride oral solutionPackage Facts
Identity
Package NDC
13107-261-58
Digits Only
1310726158
Product NDC
13107-261
Description
1 BOTTLE in 1 CARTON (13107-261-58) / 500 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
oxycodone hydrochloride oral solution
Generic
oxycodone hydrochloride oral solution
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0905edb-577e-4e2e-ab2f-c7f5c673b0e1", "openfda": {"upc": ["0313107262579", "0313107261589"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["0b3fa92e-8351-4401-860d-4bba8a7155e6"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (13107-261-58) / 500 mL in 1 BOTTLE", "package_ndc": "13107-261-58", "marketing_start_date": "20200127"}], "brand_name": "Oxycodone Hydrochloride Oral Solution", "product_id": "13107-261_b0905edb-577e-4e2e-ab2f-c7f5c673b0e1", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "13107-261", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride Oral Solution", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride Oral Solution", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA212429", "marketing_category": "ANDA", "marketing_start_date": "20200127", "listing_expiration_date": "20261231"}