Package 37808-747-71

Brand: pain relief 8 hr

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 37808-747-71
Digits Only 3780874771
Product NDC 37808-747
Description

1 BOTTLE in 1 CARTON (37808-747-71) / 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-02-24
Brand pain relief 8 hr
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6b75a346-403e-45e1-a74d-21c0b8dcd8ed", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["b5c7e93b-e626-49c3-a7d4-773475f945ae"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-747-71)  / 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "37808-747-71", "marketing_start_date": "20170224"}], "brand_name": "Pain Relief 8 HR", "product_id": "37808-747_6b75a346-403e-45e1-a74d-21c0b8dcd8ed", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "37808-747", "generic_name": "Acetaminophen", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief 8 HR", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA075077", "marketing_category": "ANDA", "marketing_start_date": "20170224", "listing_expiration_date": "20261231"}