Package 49035-278-08

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 49035-278-08
Digits Only 4903527808
Product NDC 49035-278
Description

237 mL in 1 BOTTLE, PLASTIC (49035-278-08)

Marketing

Marketing Status
Marketed Since 2015-12-31
Brand pain relief extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a330c12d-8917-4ed3-a758-735577f8c68b", "openfda": {"upc": ["0681131061261"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["872c5220-a379-4dc1-b99c-f11ebb82db35"], "manufacturer_name": ["EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (49035-278-08)", "package_ndc": "49035-278-08", "marketing_start_date": "20151231"}], "brand_name": "Pain Relief Extra Strength", "product_id": "49035-278_a330c12d-8917-4ed3-a758-735577f8c68b", "dosage_form": "LIQUID", "product_ndc": "49035-278", "generic_name": "Acetaminophen", "labeler_name": "EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20151231", "listing_expiration_date": "20261231"}