Package 43602-198-31
Brand: oxycodone hydrochloride
Generic: oxycodone hydrochloridePackage Facts
Identity
Package NDC
43602-198-31
Digits Only
4360219831
Product NDC
43602-198
Description
30 mL in 1 BOTTLE (43602-198-31)
Marketing
Marketing Status
Brand
oxycodone hydrochloride
Generic
oxycodone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46183e47-ba04-4b02-912a-6aeed41c609e", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["de96e2be-66d9-4bcb-a133-221ad32e09f1"], "manufacturer_name": ["Ascent Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (43602-198-31)", "package_ndc": "43602-198-31", "marketing_start_date": "20170713"}, {"sample": false, "description": "500 mL in 1 BOTTLE (43602-198-50)", "package_ndc": "43602-198-50", "marketing_start_date": "20170713"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "43602-198_46183e47-ba04-4b02-912a-6aeed41c609e", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "43602-198", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "Ascent Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "100 mg/5mL"}], "application_number": "ANDA209021", "marketing_category": "ANDA", "marketing_start_date": "20170713", "listing_expiration_date": "20261231"}