Package 67296-1834-1

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-1834-1
Digits Only 6729618341
Product NDC 67296-1834
Description

10 TABLET, COATED in 1 BOTTLE (67296-1834-1)

Marketing

Marketing Status
Marketed Since 2021-04-22
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": "4387f592-853f-01ea-e063-6394a90a6a4f", "openfda": {"upc": ["0372888080017", "0372888080000", "0372888008011", "0372888008004", "0372888080055", "0372888008059"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["f4c148f3-845a-61e3-e053-2a95a90a326e"], "manufacturer_name": ["RedPharm Drug Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (67296-1834-1)", "package_ndc": "67296-1834-1", "marketing_start_date": "20210422"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (67296-1834-2)", "package_ndc": "67296-1834-2", "marketing_start_date": "20210422"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (67296-1834-3)", "package_ndc": "67296-1834-3", "marketing_start_date": "20210422"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE (67296-1834-4)", "package_ndc": "67296-1834-4", "marketing_start_date": "20210422"}, {"sample": false, "description": "6 TABLET, COATED in 1 BOTTLE (67296-1834-6)", "package_ndc": "67296-1834-6", "marketing_start_date": "20210422"}, {"sample": false, "description": "15 TABLET, COATED in 1 BOTTLE (67296-1834-7)", "package_ndc": "67296-1834-7", "marketing_start_date": "20210422"}], "brand_name": "Tramadol Hydrochloride", "product_id": "67296-1834_4387f592-853f-01ea-e063-6394a90a6a4f", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-1834", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "RedPharm Drug Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA208708", "marketing_category": "ANDA", "marketing_start_date": "20210422", "listing_expiration_date": "20261231"}