Package 68180-698-06

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-698-06
Digits Only 6818069806
Product NDC 68180-698
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-698-06)

Marketing

Marketing Status
Marketed Since 2014-08-19
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": "89cbc1ac-6681-42a9-b52a-0094f9b158a8", "openfda": {"upc": ["0368180699064", "0368180697060"], "unii": ["9N7R477WCK"], "rxcui": ["833709", "833711", "833713"], "spl_set_id": ["46bb9ae6-3ee8-463c-badb-c7a45a89b84b"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-698-06)", "package_ndc": "68180-698-06", "marketing_start_date": "20140819"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "68180-698_89cbc1ac-6681-42a9-b52a-0094f9b158a8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68180-698", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20140819", "listing_expiration_date": "20271231"}