Package 51672-5319-8

Brand: feverall

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 51672-5319-8
Digits Only 5167253198
Product NDC 51672-5319
Product ID 51672-5319_38f91f45-9b1c-befa-e063-6294a90a3cc1
Description

1 BOTTLE in 1 CARTON (51672-5319-8) / 118 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-06-01
Brand feverall
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

FeverAll ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38f91f45-9b1c-befa-e063-6294a90a3cc1", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668", "2639351"], "spl_set_id": ["8970b91b-5f3c-4764-9e23-25dcb398d0a7"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-5319-8)  / 118 mL in 1 BOTTLE", "package_ndc": "51672-5319-8", "marketing_start_date": "20230601"}], "brand_name": "FeverAll", "product_id": "51672-5319_38f91f45-9b1c-befa-e063-6294a90a3cc1", "dosage_form": "SUSPENSION", "product_ndc": "51672-5319", "generic_name": "ACETAMINOPHEN", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FeverAll", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}