Package 62936-0222-5

Brand: extra strength pain reliever

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 62936-0222-5
Digits Only 6293602225
Product NDC 62936-0222
Product ID 62936-0222_115d0b60-84e9-7a34-e063-6394a90ae78c
Description

50 TABLET in 1 BOTTLE (62936-0222-5)

Marketing

Marketing Status
Marketed Since 2019-09-01
Brand extra strength pain reliever
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Extra Strength Pain Reliever ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "115d0b60-84e9-7a34-e063-6394a90ae78c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["115d0b4f-6f0f-79a9-e063-6394a90ab18a"], "manufacturer_name": ["INGLES MARKETS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62936-0222-1)", "package_ndc": "62936-0222-1", "marketing_start_date": "20190901"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (62936-0222-5)", "package_ndc": "62936-0222-5", "marketing_start_date": "20190901"}], "brand_name": "Extra Strength Pain Reliever", "product_id": "62936-0222_115d0b60-84e9-7a34-e063-6394a90ae78c", "dosage_form": "TABLET", "product_ndc": "62936-0222", "generic_name": "Acetaminophen", "labeler_name": "INGLES MARKETS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180801", "listing_expiration_date": "20261231"}