norel ad

Generic: acetaminophen, chlorpheniramine maleate, and phenylephrine hcl

Labeler: u.s. pharmaceutical corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name norel ad
Generic Name acetaminophen, chlorpheniramine maleate, and phenylephrine hcl
Labeler u.s. pharmaceutical corporation
Dosage Form TABLET, MULTILAYER
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, chlorpheniramine maleate 4 mg/1, phenylephrine hydrochloride 10 mg/1

Manufacturer
U.S. PHARMACEUTICAL CORPORATION

Identifiers & Regulatory

Product NDC 52747-475
Product ID 52747-475_41619e00-e834-2cf6-e063-6394a90a259d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2012-04-27

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52747475
Hyphenated Format 52747-475

Supplemental Identifiers

RxCUI
1193293
UPC
0352747475703
UNII
362O9ITL9D V1Q0O9OJ9Z 04JA59TNSJ

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 norel ad (source: ndc)
Generic Name acetaminophen, chlorpheniramine maleate, and phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 4 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 20 TABLET, MULTILAYER in 1 BOTTLE (52747-475-70)
source: ndc

Packages (1)

52747-475-70 20 TABLET, MULTILAYER in 1 BOTTLE (52747-475-70)

Ingredients (3)

acetaminophen (325 mg/1) chlorpheniramine maleate (4 mg/1) phenylephrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Norel AD ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41619e00-e834-2cf6-e063-6394a90a259d", "openfda": {"upc": ["0352747475703"], "unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "04JA59TNSJ"], "rxcui": ["1193293"], "spl_set_id": ["53d9ed3c-212d-4b12-ac35-8bd49382b49d"], "manufacturer_name": ["U.S. PHARMACEUTICAL CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, MULTILAYER in 1 BOTTLE (52747-475-70)", "package_ndc": "52747-475-70", "marketing_start_date": "20120427"}], "brand_name": "Norel AD", "product_id": "52747-475_41619e00-e834-2cf6-e063-6394a90a259d", "dosage_form": "TABLET, MULTILAYER", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "52747-475", "generic_name": "acetaminophen, chlorpheniramine maleate, and phenylephrine HCl", "labeler_name": "U.S. PHARMACEUTICAL CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Norel AD", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "4 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120427", "listing_expiration_date": "20261231"}