feverall

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name feverall
Generic Name acetaminophen
Labeler sun pharmaceutical industries, inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-5319
Product ID 51672-5319_38f91f45-9b1c-befa-e063-6294a90a3cc1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2023-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516725319
Hyphenated Format 51672-5319

Supplemental Identifiers

RxCUI
307668 2639351
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 (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (51672-5319-8) / 118 mL in 1 BOTTLE
source: ndc

Packages (1)

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

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

FeverAll ndc-match (0.9)

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"}