Package 0904-7496-61

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7496-61
Digits Only 0904749661
Product NDC 0904-7496
Product ID 0904-7496_82c494ed-bc8b-45f5-a26d-5e4660f79feb
Description

100 BLISTER PACK in 1 CARTON (0904-7496-61) / 1 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-11-22
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": "82c494ed-bc8b-45f5-a26d-5e4660f79feb", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["6b0b95b2-ae4c-42e8-9f2e-bcdaffda62e2"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7496-61)  / 1 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "0904-7496-61", "marketing_start_date": "20241122"}], "brand_name": "Tramadol Hydrochloride", "product_id": "0904-7496_82c494ed-bc8b-45f5-a26d-5e4660f79feb", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0904-7496", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA076003", "marketing_category": "ANDA", "marketing_start_date": "20241122", "listing_expiration_date": "20261231"}