Package 36800-770-02

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 36800-770-02
Digits Only 3680077002
Product NDC 36800-770
Product ID 36800-770_286014c1-2183-fc25-e063-6394a90aa15e
Description

1 BOTTLE, PLASTIC in 1 CARTON (36800-770-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2014-03-31
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": "286014c1-2183-fc25-e063-6394a90aa15e", "openfda": {"upc": ["0036800199903"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ecd6df7e-e7e2-446b-85ef-25971281fe31"], "manufacturer_name": ["TopCo Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-770-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "36800-770-02", "marketing_start_date": "20140331"}], "brand_name": "Pain Relief Extra Strength", "product_id": "36800-770_286014c1-2183-fc25-e063-6394a90aa15e", "dosage_form": "TABLET, COATED", "product_ndc": "36800-770", "generic_name": "Acetaminophen", "labeler_name": "TopCo Associates LLC", "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": "20140331", "listing_expiration_date": "20261231"}