Package 42806-627-01
Brand: tapentadol hydrochloride
Generic: tapentadol hydrochloridePackage Facts
Identity
Package NDC
42806-627-01
Digits Only
4280662701
Product NDC
42806-627
Description
100 TABLET, FILM COATED in 1 BOTTLE (42806-627-01)
Marketing
Marketing Status
Brand
tapentadol hydrochloride
Generic
tapentadol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "120aa46b-8c91-4460-8e91-85cbaac53d20", "openfda": {"upc": ["0342806628010", "0342806626016", "0342806627013"], "unii": ["71204KII53"], "rxcui": ["825409", "825411", "825413"], "spl_set_id": ["fecd2104-5bf3-47ed-a6f0-5c6ebb0a17b4"], "manufacturer_name": ["EPIC PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-627-01)", "package_ndc": "42806-627-01", "marketing_start_date": "20211231"}], "brand_name": "Tapentadol Hydrochloride", "product_id": "42806-627_120aa46b-8c91-4460-8e91-85cbaac53d20", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "42806-627", "dea_schedule": "CII", "generic_name": "Tapentadol Hydrochloride", "labeler_name": "EPIC PHARMA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tapentadol Hydrochloride", "active_ingredients": [{"name": "TAPENTADOL HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA214378", "marketing_category": "ANDA", "marketing_start_date": "20211231", "listing_expiration_date": "20271231"}