Package 0615-8560-39
Brand: acamprosate calcium
Generic: acamprosate calcium enteric-coatedPackage Facts
Identity
Package NDC
0615-8560-39
Digits Only
0615856039
Product NDC
0615-8560
Description
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8560-39)
Marketing
Marketing Status
Brand
acamprosate calcium
Generic
acamprosate calcium enteric-coated
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "190e50c0-f4c7-408b-b3b3-99c0b3647164", "openfda": {"unii": ["59375N1D0U"], "rxcui": ["835726"], "spl_set_id": ["f2bf6742-4b85-45e2-8daa-0f9bfc75a128"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8560-39)", "package_ndc": "0615-8560-39", "marketing_start_date": "20250218"}], "brand_name": "Acamprosate Calcium", "product_id": "0615-8560_190e50c0-f4c7-408b-b3b3-99c0b3647164", "dosage_form": "TABLET, DELAYED RELEASE", "product_ndc": "0615-8560", "generic_name": "acamprosate calcium enteric-coated", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acamprosate Calcium", "active_ingredients": [{"name": "ACAMPROSATE CALCIUM", "strength": "333 mg/1"}], "application_number": "ANDA200142", "marketing_category": "ANDA", "marketing_start_date": "20140924", "listing_expiration_date": "20261231"}