Package 37808-704-02

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 37808-704-02
Digits Only 3780870402
Product NDC 37808-704
Product ID 37808-704_24fdff52-1508-44f6-e063-6394a90a5a53
Description

1 BOTTLE, PLASTIC in 1 CARTON (37808-704-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2013-02-01
Brand pain relief extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24fdff52-1508-44f6-e063-6394a90a5a53", "openfda": {"upc": ["0041220278572"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["f17a18b0-a7c2-4c64-868c-460cf34e1f7d"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-704-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-704-02", "marketing_start_date": "20130201"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (37808-704-09)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-704-09", "marketing_start_date": "20110101"}], "brand_name": "Pain Relief Extra Strength", "product_id": "37808-704_24fdff52-1508-44f6-e063-6394a90a5a53", "dosage_form": "TABLET, COATED", "product_ndc": "37808-704", "generic_name": "Acetaminophen", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110101", "listing_expiration_date": "20261231"}