alavert allergy

Generic: loratadine

Labeler: foundation consumer healthcare
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alavert allergy
Generic Name loratadine
Labeler foundation consumer healthcare
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Foundation Consumer Healthcare

Identifiers & Regulatory

Product NDC 69536-195
Product ID 69536-195_1ba62e9b-1b1f-016a-e063-6394a90a065e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213294
Listing Expiration 2026-12-31
Marketing Start 2024-10-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69536195
Hyphenated Format 69536-195

Supplemental Identifiers

RxCUI
311373 351855
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 alavert allergy (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA213294 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 CARTON (69536-195-20) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
  • 60 BLISTER PACK in 1 CARTON (69536-195-60) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
source: ndc

Packages (2)

69536-195-20 20 BLISTER PACK in 1 CARTON (69536-195-20) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK 69536-195-60 60 BLISTER PACK in 1 CARTON (69536-195-60) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Alavert Allergy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1ba62e9b-1b1f-016a-e063-6394a90a065e", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311373", "351855"], "spl_set_id": ["1704474a-9b99-de45-e063-6294a90ac59b"], "manufacturer_name": ["Foundation Consumer Healthcare"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (69536-195-20)  / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "69536-195-20", "marketing_start_date": "20241031"}, {"sample": false, "description": "60 BLISTER PACK in 1 CARTON (69536-195-60)  / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "69536-195-60", "marketing_start_date": "20241031"}], "brand_name": "Alavert Allergy", "product_id": "69536-195_1ba62e9b-1b1f-016a-e063-6394a90a065e", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "69536-195", "generic_name": "LORATADINE", "labeler_name": "Foundation Consumer Healthcare", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alavert", "brand_name_suffix": "Allergy", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA213294", "marketing_category": "ANDA", "marketing_start_date": "20241031", "listing_expiration_date": "20261231"}