Package 43386-920-60

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43386-920-60
Digits Only 4338692060
Product NDC 43386-920
Product ID 43386-920_e5a8251c-8fc6-4b34-a01f-1706ebda9f94
Description

1 BOTTLE in 1 CARTON (43386-920-60) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2015-04-29
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": "e5a8251c-8fc6-4b34-a01f-1706ebda9f94", "openfda": {"upc": ["0343386920600"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049615"], "spl_set_id": ["3eddd18b-695a-4e53-a76c-f6779515b918"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (43386-920-60)  / 30 mL in 1 BOTTLE", "package_ndc": "43386-920-60", "marketing_start_date": "20150429"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "43386-920_e5a8251c-8fc6-4b34-a01f-1706ebda9f94", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "43386-920", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA204603", "marketing_category": "ANDA", "marketing_start_date": "20150429", "listing_expiration_date": "20261231"}