Package 71205-708-90

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-708-90
Digits Only 7120570890
Product NDC 71205-708
Product ID 71205-708_00b7f61b-5173-43e6-a3f9-d2efbda40c19
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)

Marketing

Marketing Status
Marketed Since 2022-10-31
Brand tramadol hydrochloride
Generic tramadol hydrochloride
Sample Package No

Linked Drug Pages (1)

TRAMADOL HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "00b7f61b-5173-43e6-a3f9-d2efbda40c19", "openfda": {"upc": ["0371205708306"], "unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["00b7f61b-5173-43e6-a3f9-d2efbda40c19"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-30)", "package_ndc": "71205-708-30", "marketing_start_date": "20221031"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-60)", "package_ndc": "71205-708-60", "marketing_start_date": "20221031"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)", "package_ndc": "71205-708-90", "marketing_start_date": "20221031"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "71205-708_00b7f61b-5173-43e6-a3f9-d2efbda40c19", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71205-708", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA201384", "marketing_category": "ANDA", "marketing_start_date": "20111212", "listing_expiration_date": "20261231"}