Package 11822-0812-2

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 11822-0812-2
Digits Only 1182208122
Product NDC 11822-0812
Product ID 11822-0812_11f0d173-9b0e-4de3-9f25-73186fee995d
Description

1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-2) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 1993-04-02
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": "11f0d173-9b0e-4de3-9f25-73186fee995d", "openfda": {"upc": ["0011822365673"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["d846065a-5c39-4f4b-894c-4280acaaf4fa"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-2)  / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-0812-2", "marketing_start_date": "19930402"}], "brand_name": "Pain Relief Extra Strength", "product_id": "11822-0812_11f0d173-9b0e-4de3-9f25-73186fee995d", "dosage_form": "TABLET, FILM COATED", "product_ndc": "11822-0812", "generic_name": "Acetaminophen", "labeler_name": "Rite Aid Corporation", "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": "19930402", "listing_expiration_date": "20261231"}