Package 13107-261-58

Brand: oxycodone hydrochloride oral solution

Generic: oxycodone hydrochloride oral solution
NDC Package

Package 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
Marketed Since 2020-01-27
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"}