Package 63941-192-01

Brand: extra strength pain relief

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63941-192-01
Digits Only 6394119201
Product NDC 63941-192
Description

1 BOTTLE, PLASTIC in 1 CARTON (63941-192-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2028-04-30
Brand extra strength 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": "45b2229e-ea1e-92d0-e063-6294a90a9e82", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["d4c32e70-778a-4d66-b9d0-03944a528421"], "manufacturer_name": ["VALU MERCHANDISERS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-192-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-192-01", "marketing_end_date": "20280430", "marketing_start_date": "20070619"}], "brand_name": "Extra Strength Pain Relief", "product_id": "63941-192_45b2229e-ea1e-92d0-e063-6294a90a9e82", "dosage_form": "TABLET, COATED", "product_ndc": "63941-192", "generic_name": "Acetaminophen", "labeler_name": "VALU MERCHANDISERS COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20280430", "marketing_start_date": "20070619"}