Package 69452-353-25
Brand: acamprosate calcium
Generic: acamprosate calciumPackage Facts
Identity
Package NDC
69452-353-25
Digits Only
6945235325
Product NDC
69452-353
Description
180 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-353-25)
Marketing
Marketing Status
Brand
acamprosate calcium
Generic
acamprosate calcium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44732224-b730-9a24-e063-6394a90ac0c0", "openfda": {"unii": ["59375N1D0U"], "rxcui": ["835726"], "spl_set_id": ["4473326f-79f1-61b2-e063-6294a90a17a3"], "manufacturer_name": ["Bionpharma Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-353-25)", "package_ndc": "69452-353-25", "marketing_start_date": "20251201"}], "brand_name": "Acamprosate Calcium", "product_id": "69452-353_44732224-b730-9a24-e063-6394a90ac0c0", "dosage_form": "TABLET, DELAYED RELEASE", "product_ndc": "69452-353", "generic_name": "Acamprosate Calcium", "labeler_name": "Bionpharma Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acamprosate Calcium", "active_ingredients": [{"name": "ACAMPROSATE CALCIUM", "strength": "333 mg/1"}], "application_number": "ANDA219904", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}