all day allergy relief

Generic: loratadine

Labeler: quality choice (chain drug marketing association)
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day allergy relief
Generic Name loratadine
Labeler quality choice (chain drug marketing association)
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
QUALITY CHOICE (Chain Drug Marketing Association)

Identifiers & Regulatory

Product NDC 83324-146
Product ID 83324-146_eb859e8d-d4f6-4823-8ce8-fa51f6f2245e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075209
Listing Expiration 2026-12-31
Marketing Start 2024-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324146
Hyphenated Format 83324-146

Supplemental Identifiers

RxCUI
311372
UPC
0635515997356
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 all day allergy relief (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA075209 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (83324-146-30) / 30 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb859e8d-d4f6-4823-8ce8-fa51f6f2245e", "openfda": {"upc": ["0635515997356"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["a282d209-1015-4570-b9df-7cc0a3753e37"], "manufacturer_name": ["QUALITY CHOICE (Chain Drug Marketing Association)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (83324-146-30)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "83324-146-30", "marketing_start_date": "20240731"}], "brand_name": "All Day Allergy Relief", "product_id": "83324-146_eb859e8d-d4f6-4823-8ce8-fa51f6f2245e", "dosage_form": "TABLET", "product_ndc": "83324-146", "generic_name": "Loratadine", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Allergy Relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA075209", "marketing_category": "ANDA", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}