Package 52817-615-16

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 52817-615-16
Digits Only 5281761516
Product NDC 52817-615
Description

473 mL in 1 BOTTLE (52817-615-16)

Marketing

Marketing Status
Marketed Since 2023-01-25
Brand tramadol hydrochloride
Generic tramadol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f7fd27bd-cd40-704c-e053-6394a90a6a6f", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["2395808"], "spl_set_id": ["aea56ff9-94ac-47a8-8f15-8790d538973b"], "manufacturer_name": ["TruPharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (52817-615-16)", "package_ndc": "52817-615-16", "marketing_start_date": "20230125"}], "brand_name": "Tramadol Hydrochloride", "product_id": "52817-615_f7fd27bd-cd40-704c-e053-6394a90a6a6f", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "52817-615", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "TruPharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "NDA214044", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200911", "listing_expiration_date": "20261231"}