Package 49483-697-43
Brand: extra strength acetaminophen
Generic: acetaminophenPackage Facts
Identity
Package NDC
49483-697-43
Digits Only
4948369743
Product NDC
49483-697
Description
400 TABLET in 1 BOTTLE (49483-697-43)
Marketing
Marketing Status
Brand
extra strength acetaminophen
Generic
acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2dc52443-77b2-5143-e063-6394a90a4958", "openfda": {"upc": ["0349483697438"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["c9f80d24-bd05-e1ce-e053-2995a90aa646"], "manufacturer_name": ["TIME CAP LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET in 1 BOTTLE (49483-697-43)", "package_ndc": "49483-697-43", "marketing_start_date": "20220211"}], "brand_name": "EXTRA STRENGTH ACETAMINOPHEN", "product_id": "49483-697_2dc52443-77b2-5143-e063-6394a90a4958", "dosage_form": "TABLET", "product_ndc": "49483-697", "generic_name": "Acetaminophen", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220211", "listing_expiration_date": "20261231"}