Package 68071-5142-2

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5142-2
Digits Only 6807151422
Product NDC 68071-5142
Description

12 TABLET in 1 BOTTLE (68071-5142-2)

Marketing

Marketing Status
Marketed Since 2020-01-08
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": "1b54c8e7-282d-91f2-e063-6394a90a1db7", "openfda": {"upc": ["0368071514261"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["9ba9c68c-ff27-eb24-e053-2a95a90ae21c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68071-5142-2)", "package_ndc": "68071-5142-2", "marketing_start_date": "20200108"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-5142-6)", "package_ndc": "68071-5142-6", "marketing_start_date": "20200108"}], "brand_name": "tramadol hydrochloride", "product_id": "68071-5142_1b54c8e7-282d-91f2-e063-6394a90a1db7", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-5142", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tramadol hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075964", "marketing_category": "ANDA", "marketing_start_date": "20020622", "listing_expiration_date": "20261231"}