Package 68998-198-02

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 68998-198-02
Digits Only 6899819802
Product NDC 68998-198
Product ID 68998-198_2526421a-bb29-1e0b-e063-6394a90a42fc
Description

1 BOTTLE, PLASTIC in 1 CARTON (68998-198-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2022-10-05
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": "2526421a-bb29-1e0b-e063-6394a90a42fc", "openfda": {"upc": ["0094442601079"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["e231c2f6-927c-1ab0-e053-2995a90a6121"], "manufacturer_name": ["MARC GLASSMAN, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68998-198-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68998-198-02", "marketing_start_date": "20221005"}], "brand_name": "Pain Relief Extra Strength", "product_id": "68998-198_2526421a-bb29-1e0b-e063-6394a90a42fc", "dosage_form": "TABLET, COATED", "product_ndc": "68998-198", "generic_name": "Acetaminophen", "labeler_name": "MARC GLASSMAN, INC.", "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": "20221005", "listing_expiration_date": "20261231"}