Package 51672-2114-4

Brand: feverall infants

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 51672-2114-4
Digits Only 5167221144
Product NDC 51672-2114
Product ID 51672-2114_49e3a7b2-e928-d275-e063-6394a90a70c3
Description

50 BLISTER PACK in 1 CARTON (51672-2114-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)

Marketing

Marketing Status
Marketed Since 2013-12-12
Brand feverall infants
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Feverall Infants ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RECTAL"], "spl_id": "49e3a7b2-e928-d275-e063-6394a90a70c3", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198445", "209531"], "spl_set_id": ["3ade895b-5dca-4d81-9415-8091923162ff"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (51672-2114-2)  / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)", "package_ndc": "51672-2114-2", "marketing_start_date": "20131212"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (51672-2114-4)  / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)", "package_ndc": "51672-2114-4", "marketing_start_date": "20131212"}], "brand_name": "Feverall Infants", "product_id": "51672-2114_49e3a7b2-e928-d275-e063-6394a90a70c3", "dosage_form": "SUPPOSITORY", "product_ndc": "51672-2114", "generic_name": "Acetaminophen", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Feverall", "brand_name_suffix": "Infants", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "80 mg/1"}], "application_number": "NDA018337", "marketing_category": "NDA", "marketing_start_date": "20131212", "listing_expiration_date": "20271231"}