Package 72189-521-30

Brand: tramadol hcl er

Generic: tramadol hcl er
NDC Package

Package Facts

Identity

Package NDC 72189-521-30
Digits Only 7218952130
Product NDC 72189-521
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-521-30)

Marketing

Marketing Status
Marketed Since 2023-11-08
Brand tramadol hcl er
Generic tramadol hcl er
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4e6900-1d19-f1d7-e063-6394a90a16d5", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833713"], "spl_set_id": ["09a7af47-423a-1e8b-e063-6394a90a99ef"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-521-30)", "package_ndc": "72189-521-30", "marketing_start_date": "20231108"}], "brand_name": "Tramadol HCL ER", "product_id": "72189-521_2c4e6900-1d19-f1d7-e063-6394a90a16d5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-521", "dea_schedule": "CIV", "generic_name": "Tramadol HCL ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol HCL ER", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20231108", "listing_expiration_date": "20261231"}