loratadine allergy relief

Generic: loratadine

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

Drug Facts

Product Profile

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

loratadine 10 mg/1

Manufacturer
OHM LABORATORIES INC.

Identifiers & Regulatory

Product NDC 51660-526
Product ID 51660-526_ab379305-5823-49e9-89ca-641c1d37a6f3
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076134
Listing Expiration 2026-12-31
Marketing Start 2017-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51660526
Hyphenated Format 51660-526

Supplemental Identifiers

RxCUI
311372
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 allergy relief (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA076134 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (51660-526-01)
  • 500 TABLET in 1 BOTTLE (51660-526-05)
  • 10 TABLET in 1 BLISTER PACK (51660-526-11)
  • 30 TABLET in 1 BOTTLE (51660-526-30)
  • 30 TABLET in 1 BLISTER PACK (51660-526-31)
  • 300 TABLET in 1 BOTTLE (51660-526-53)
source: ndc

Packages (6)

51660-526-01 100 TABLET in 1 BOTTLE (51660-526-01) 51660-526-05 500 TABLET in 1 BOTTLE (51660-526-05) 51660-526-11 10 TABLET in 1 BLISTER PACK (51660-526-11) 51660-526-30 30 TABLET in 1 BOTTLE (51660-526-30) 51660-526-31 30 TABLET in 1 BLISTER PACK (51660-526-31) 51660-526-53 300 TABLET in 1 BOTTLE (51660-526-53)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Loratadine Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ab379305-5823-49e9-89ca-641c1d37a6f3", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["c35f2cc1-f76d-4824-b0a5-747bca0c3b85"], "manufacturer_name": ["OHM LABORATORIES INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51660-526-01)", "package_ndc": "51660-526-01", "marketing_start_date": "20171101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (51660-526-05)", "package_ndc": "51660-526-05", "marketing_start_date": "20171101"}, {"sample": false, "description": "10 TABLET in 1 BLISTER PACK (51660-526-11)", "package_ndc": "51660-526-11", "marketing_start_date": "20171101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51660-526-30)", "package_ndc": "51660-526-30", "marketing_start_date": "20190201"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (51660-526-31)", "package_ndc": "51660-526-31", "marketing_start_date": "20171101"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (51660-526-53)", "package_ndc": "51660-526-53", "marketing_start_date": "20171101"}], "brand_name": "Loratadine Allergy Relief", "product_id": "51660-526_ab379305-5823-49e9-89ca-641c1d37a6f3", "dosage_form": "TABLET", "product_ndc": "51660-526", "generic_name": "Loratadine", "labeler_name": "OHM LABORATORIES INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine Allergy Relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076134", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20261231"}