loratadine

Generic: loratadine

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler rite aid corporation
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-0919
Product ID 11822-0919_754e27cd-8990-46b7-9325-16e1765c0807
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076011
Listing Expiration 2026-12-31
Marketing Start 2020-09-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118220919
Hyphenated Format 11822-0919

Supplemental Identifiers

RxCUI
311373
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 loratadine (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA076011 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (11822-0919-0) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
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": "754e27cd-8990-46b7-9325-16e1765c0807", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311373"], "spl_set_id": ["004dd408-e3ff-4ba6-b859-beebe364f0e1"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (11822-0919-0)  / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "11822-0919-0", "marketing_start_date": "20200925"}], "brand_name": "loratadine", "product_id": "11822-0919_754e27cd-8990-46b7-9325-16e1765c0807", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "11822-0919", "generic_name": "loratadine", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076011", "marketing_category": "ANDA", "marketing_start_date": "20200925", "listing_expiration_date": "20261231"}