Package 69842-878-08

Brand: pain reliever fever reducer extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 69842-878-08
Digits Only 6984287808
Product NDC 69842-878
Product ID 69842-878_e15ec20e-e4d2-485c-a8df-0c2fd096d2eb
Description

237 mL in 1 BOTTLE, PLASTIC (69842-878-08)

Marketing

Marketing Status
Marketed Since 2018-04-30
Brand pain reliever fever reducer extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Reliever fever Reducer Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e15ec20e-e4d2-485c-a8df-0c2fd096d2eb", "openfda": {"upc": ["0050428260944"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["7b5263ad-01b7-4fc5-9384-4da8efe89e35"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (69842-878-08)", "package_ndc": "69842-878-08", "marketing_start_date": "20180430"}], "brand_name": "Pain Reliever fever Reducer Extra Strength", "product_id": "69842-878_e15ec20e-e4d2-485c-a8df-0c2fd096d2eb", "dosage_form": "LIQUID", "product_ndc": "69842-878", "generic_name": "Acetaminophen", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever fever Reducer", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180430", "listing_expiration_date": "20261231"}