Package 66715-9637-4

Brand: pain reliever

Generic: acetaminophen tablet, extra strength
NDC Package

Package Facts

Identity

Package NDC 66715-9637-4
Digits Only 6671596374
Product NDC 66715-9637
Description

10 TABLET, FILM COATED in 1 VIAL, PLASTIC (66715-9637-4)

Marketing

Marketing Status
Marketed Since 2022-09-30
Brand pain reliever
Generic acetaminophen tablet, extra strength
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c8f99ae-73a5-7ac4-e063-6294a90a0f36", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["f0fdab5a-9d07-57aa-e053-2a95a90adc7f"], "manufacturer_name": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 VIAL, PLASTIC (66715-9637-4)", "package_ndc": "66715-9637-4", "marketing_start_date": "20220930"}], "brand_name": "Pain Reliever", "product_id": "66715-9637_0c8f99ae-73a5-7ac4-e063-6294a90a0f36", "dosage_form": "TABLET, FILM COATED", "product_ndc": "66715-9637", "generic_name": "acetaminophen tablet, extra strength", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220930", "listing_expiration_date": "20261231"}