up and up childrens allergy

Generic: loratadine

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up childrens allergy
Generic Name loratadine
Labeler target corporation
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

loratadine 5 mg/5mL

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 82442-207
Product ID 82442-207_36a8b979-6403-4545-82e0-d3bccdd2654e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075728
Listing Expiration 2026-12-31
Marketing Start 2024-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82442207
Hyphenated Format 82442-207

Supplemental Identifiers

RxCUI
692783
UNII
7AJO3BO7QN

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 up and up childrens allergy (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA075728 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (82442-207-26) / 120 mL in 1 BOTTLE
source: ndc

Packages (1)

82442-207-26 1 BOTTLE in 1 CARTON (82442-207-26) / 120 mL in 1 BOTTLE

Ingredients (1)

loratadine (5 mg/5mL)

Linked Drug Pages (1)

UP AND UP CHILDRENS ALLERGY ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "36a8b979-6403-4545-82e0-d3bccdd2654e", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["692783"], "spl_set_id": ["a9f6ae02-cf29-4111-99e7-7e6b1ecb88f0"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82442-207-26)  / 120 mL in 1 BOTTLE", "package_ndc": "82442-207-26", "marketing_start_date": "20240731"}], "brand_name": "UP AND UP CHILDRENS ALLERGY", "product_id": "82442-207_36a8b979-6403-4545-82e0-d3bccdd2654e", "dosage_form": "SOLUTION", "product_ndc": "82442-207", "generic_name": "Loratadine", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UP AND UP CHILDRENS ALLERGY", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/5mL"}], "application_number": "ANDA075728", "marketing_category": "ANDA", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}