Package 51672-2115-4

Brand: feverall childrens

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 51672-2115-4
Digits Only 5167221154
Product NDC 51672-2115
Product ID 51672-2115_49e3a099-4616-d038-e063-6394a90a90a6
Description

50 BLISTER PACK in 1 CARTON (51672-2115-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2115-0)

Marketing

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

Linked Drug Pages (1)

Feverall Childrens ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RECTAL"], "spl_id": "49e3a099-4616-d038-e063-6394a90a90a6", "openfda": {"upc": ["0351672211523"], "unii": ["362O9ITL9D"], "rxcui": ["198434", "209353"], "spl_set_id": ["861e2987-5473-45b0-b2a6-f980a9b0e809"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (51672-2115-2)  / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2115-0)", "package_ndc": "51672-2115-2", "marketing_start_date": "20131212"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (51672-2115-4)  / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2115-0)", "package_ndc": "51672-2115-4", "marketing_start_date": "20131212"}], "brand_name": "Feverall Childrens", "product_id": "51672-2115_49e3a099-4616-d038-e063-6394a90a90a6", "dosage_form": "SUPPOSITORY", "product_ndc": "51672-2115", "generic_name": "Acetaminophen", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Feverall", "brand_name_suffix": "Childrens", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "120 mg/1"}], "application_number": "NDA018337", "marketing_category": "NDA", "marketing_start_date": "20131212", "listing_expiration_date": "20271231"}