Package 37808-195-08

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 37808-195-08
Digits Only 3780819508
Product NDC 37808-195
Description

1 BOTTLE, PLASTIC in 1 CARTON (37808-195-08) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2004-05-10
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": "eef88a02-d62d-47e1-85f1-16d3d20e86d1", "openfda": {"upc": ["0041220359882"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["99699cd6-ba7d-4db0-9f0f-0f2c1a369138"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-195-08)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-195-08", "marketing_start_date": "20040510"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-195-12)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-195-12", "marketing_start_date": "20040510"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-195-20)", "package_ndc": "37808-195-20", "marketing_start_date": "20040510"}], "brand_name": "Pain Relief Extra Strength", "product_id": "37808-195_eef88a02-d62d-47e1-85f1-16d3d20e86d1", "dosage_form": "TABLET, COATED", "product_ndc": "37808-195", "generic_name": "Acetaminophen", "labeler_name": "H E B", "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": "20040510", "listing_expiration_date": "20271231"}