Package 60687-795-01

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-795-01
Digits Only 6068779501
Product NDC 60687-795
Product ID 60687-795_3d5c1244-dda1-8f70-e063-6394a90a4e38
Description

100 BLISTER PACK in 1 CARTON (60687-795-01) / 1 TABLET, COATED in 1 BLISTER PACK (60687-795-11)

Marketing

Marketing Status
Marketed Since 2024-01-20
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": "3d5c1244-dda1-8f70-e063-6394a90a4e38", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["f6f6069b-cc75-4b87-afa5-b83001b543e0"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-795-01)  / 1 TABLET, COATED in 1 BLISTER PACK (60687-795-11)", "package_ndc": "60687-795-01", "marketing_start_date": "20240120"}], "brand_name": "Tramadol Hydrochloride", "product_id": "60687-795_3d5c1244-dda1-8f70-e063-6394a90a4e38", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60687-795", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "American Health Packaging", "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": "20240120", "listing_expiration_date": "20261231"}