Package 0093-3301-01

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-3301-01
Digits Only 0093330101
Product NDC 0093-3301
Product ID 0093-3301_502158c7-0bbc-4818-aa36-c6532bde9110
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-3301-01)

Marketing

Marketing Status
Marketed Since 2024-09-17
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": "502158c7-0bbc-4818-aa36-c6532bde9110", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["561f00e5-f69c-4369-ae4d-5eff86c4499f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-3301-01)", "package_ndc": "0093-3301-01", "marketing_start_date": "20240917"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-3301-05)", "package_ndc": "0093-3301-05", "marketing_start_date": "20240912"}], "brand_name": "Tramadol Hydrochloride", "product_id": "0093-3301_502158c7-0bbc-4818-aa36-c6532bde9110", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0093-3301", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075977", "marketing_category": "ANDA", "marketing_start_date": "20240912", "listing_expiration_date": "20271231"}