feverall infants

Generic: acetaminophen

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name feverall infants
Generic Name acetaminophen
Labeler sun pharmaceutical industries, inc.
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

acetaminophen 80 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-2114
Product ID 51672-2114_49e3a7b2-e928-d275-e063-6394a90a70c3
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA018337
Listing Expiration 2027-12-31
Marketing Start 2013-12-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516722114
Hyphenated Format 51672-2114

Supplemental Identifiers

RxCUI
198445 209531
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name feverall infants (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number NDA018337 (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 6 BLISTER PACK in 1 CARTON (51672-2114-2) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)
  • 50 BLISTER PACK in 1 CARTON (51672-2114-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)
source: ndc

Packages (2)

51672-2114-2 6 BLISTER PACK in 1 CARTON (51672-2114-2) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0) 51672-2114-4 50 BLISTER PACK in 1 CARTON (51672-2114-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)

Ingredients (1)

acetaminophen (80 mg/1)

Linked Drug Pages (1)

Feverall Infants ndc-match (0.9)

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"}