Package 41250-966-47
Brand: arthritis pain relief
Generic: acetaminophenPackage Facts
Identity
Package NDC
41250-966-47
Digits Only
4125096647
Product NDC
41250-966
Description
150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (41250-966-47)
Marketing
Marketing Status
Brand
arthritis pain relief
Generic
acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a80c0c5f-8bf9-4d1f-99cf-efd421d3db1a", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["c388f3a5-03bb-4fed-b81a-bb876bc260f0"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (41250-966-47)", "package_ndc": "41250-966-47", "marketing_start_date": "20070905"}], "brand_name": "arthritis pain relief", "product_id": "41250-966_a80c0c5f-8bf9-4d1f-99cf-efd421d3db1a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "41250-966", "generic_name": "Acetaminophen", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "arthritis pain relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA075077", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}