Package 70752-137-03

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70752-137-03
Digits Only 7075213703
Product NDC 70752-137
Product ID 70752-137_16bbc411-6512-4799-a12d-12b7f3572afe
Description

1 BOTTLE in 1 CARTON (70752-137-03) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-06-02
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "16bbc411-6512-4799-a12d-12b7f3572afe", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["391701e5-2035-43fa-91ce-d27a1af19492"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70752-137-03)  / 30 mL in 1 BOTTLE", "package_ndc": "70752-137-03", "marketing_start_date": "20210602"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "70752-137_16bbc411-6512-4799-a12d-12b7f3572afe", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70752-137", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "100 mg/5mL"}], "application_number": "ANDA213761", "marketing_category": "ANDA", "marketing_start_date": "20210602", "listing_expiration_date": "20261231"}