claritin

Generic: loratadine

Labeler: navajo manufacturing company
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name claritin
Generic Name loratadine
Labeler navajo manufacturing company
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Navajo Manufacturing Company

Identifiers & Regulatory

Product NDC 67751-153
Product ID 67751-153_f5db87e3-16ba-4e7e-e053-2995a90ab04e
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA019658
Listing Expiration 2026-12-31
Marketing Start 2017-12-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67751153
Hyphenated Format 67751-153

Supplemental Identifiers

RxCUI
206805 311372
UPC
0024291262459
UNII
7AJO3BO7QN

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 claritin (source: ndc)
Generic Name loratadine (source: ndc)
Application Number NDA019658 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • Principle Display Panel - 12 Pouch Dispensit Principle Display Panel - 12 Pouch Dispensit
source: label

Packages (0)

No package records.

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (2)

Claritin ndc-match (0.9) Claritin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f5db87e3-16ba-4e7e-e053-2995a90ab04e", "openfda": {"upc": ["0024291262459"], "unii": ["7AJO3BO7QN"], "rxcui": ["206805", "311372"], "spl_set_id": ["60a5dc14-3f74-8414-e053-2991aa0ad34a"], "manufacturer_name": ["Navajo Manufacturing Company"]}, "finished": true, "packaging": [], "brand_name": "Claritin", "product_id": "67751-153_f5db87e3-16ba-4e7e-e053-2995a90ab04e", "dosage_form": "TABLET", "product_ndc": "67751-153", "generic_name": "loratadine", "labeler_name": "Navajo Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Claritin", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "NDA019658", "marketing_category": "NDA", "marketing_start_date": "20171204", "listing_expiration_date": "20261231"}