Package 49580-3278-8

Brand: pain reliever extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 49580-3278-8
Digits Only 4958032788
Product NDC 49580-3278
Product ID 49580-3278_5a915cb3-5df8-4967-9290-b1dc797ec257
Description

237 mL in 1 BOTTLE, PLASTIC (49580-3278-8)

Marketing

Marketing Status
Marketed Since 2019-11-29
Brand pain reliever extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Reliever Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5a915cb3-5df8-4967-9290-b1dc797ec257", "openfda": {"upc": ["0349580278080"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["061df1fd-173a-4bd1-9600-540ac0f3964d"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (49580-3278-8)", "package_ndc": "49580-3278-8", "marketing_start_date": "20191129"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "49580-3278_5a915cb3-5df8-4967-9290-b1dc797ec257", "dosage_form": "LIQUID", "product_ndc": "49580-3278", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191129", "listing_expiration_date": "20261231"}