all day allergy relief

Generic: loratadine

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day allergy relief
Generic Name loratadine
Labeler p & l development, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-915
Product ID 59726-915_1a4f8278-eb88-4f8e-b419-c2abb5328f28
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075209
Listing Expiration 2026-12-31
Marketing Start 2019-10-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59726915
Hyphenated Format 59726-915

Supplemental Identifiers

RxCUI
311372
UPC
0359726915908
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
  • 10 BLISTER PACK in 1 CARTON (59726-915-10) / 1 TABLET in 1 BLISTER PACK
  • 30 TABLET in 1 BOTTLE, PLASTIC (59726-915-30)
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-915-90) / 90 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a4f8278-eb88-4f8e-b419-c2abb5328f28", "openfda": {"upc": ["0359726915908"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["15ac4116-ed68-40c0-936c-7be1ef141249"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (59726-915-10)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "59726-915-10", "marketing_start_date": "20191030"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (59726-915-30)", "package_ndc": "59726-915-30", "marketing_start_date": "20191030"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-915-90)  / 90 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-915-90", "marketing_start_date": "20191030"}], "brand_name": "All Day Allergy Relief", "product_id": "59726-915_1a4f8278-eb88-4f8e-b419-c2abb5328f28", "dosage_form": "TABLET", "product_ndc": "59726-915", "generic_name": "Loratadine", "labeler_name": "P & L Development, LLC", "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": "20191030", "listing_expiration_date": "20261231"}