allergy relief

Generic: loratadine

Labeler: ohm laboratories inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name loratadine
Labeler ohm laboratories inc.
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Ohm Laboratories Inc.

Identifiers & Regulatory

Product NDC 51660-527
Product ID 51660-527_7b87d8ea-1102-4642-8a39-b2504dbda716
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077153
Listing Expiration 2026-12-31
Marketing Start 2007-08-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51660527
Hyphenated Format 51660-527

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 allergy relief (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA077153 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (51660-527-31) / 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": "7b87d8ea-1102-4642-8a39-b2504dbda716", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311373"], "spl_set_id": ["de3a7725-5d1b-4195-a9f8-43f92888997c"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (51660-527-31)  / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "51660-527-31", "marketing_start_date": "20070831"}], "brand_name": "Allergy Relief", "product_id": "51660-527_7b87d8ea-1102-4642-8a39-b2504dbda716", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "51660-527", "generic_name": "Loratadine", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA077153", "marketing_category": "ANDA", "marketing_start_date": "20070831", "listing_expiration_date": "20261231"}