loratadine

Generic: loratadine

Labeler: apotex corp.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler apotex corp.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-0147
Product ID 60505-0147_c15c5b51-bc6a-e99e-e5e7-52e61c5da7b0
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076471
Listing Expiration 2026-12-31
Marketing Start 2005-01-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605050147
Hyphenated Format 60505-0147

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 (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA076471 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (60505-0147-8)
source: ndc

Packages (1)

60505-0147-8 1000 TABLET in 1 BOTTLE (60505-0147-8)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Loratadine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c15c5b51-bc6a-e99e-e5e7-52e61c5da7b0", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["679164cc-7505-7ed4-13fe-87f06cb777d8"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (60505-0147-8)", "package_ndc": "60505-0147-8", "marketing_start_date": "20050124"}], "brand_name": "Loratadine", "product_id": "60505-0147_c15c5b51-bc6a-e99e-e5e7-52e61c5da7b0", "dosage_form": "TABLET", "product_ndc": "60505-0147", "generic_name": "Loratadine", "labeler_name": "Apotex Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076471", "marketing_category": "ANDA", "marketing_start_date": "20050124", "listing_expiration_date": "20261231"}