claritin

Generic: loratadine

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

Drug Facts

Product Profile

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

loratadine 10 mg/1

Manufacturer
Navajo Manufacturing Company Inc.

Identifiers & Regulatory

Product NDC 67751-153
Product ID 67751-153_f5db88bd-8ea6-0df0-e053-2995a90a18b4
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA019658
Listing Expiration 2026-12-31
Marketing Start 2016-09-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67751153
Hyphenated Format 67751-153

Supplemental Identifiers

RxCUI
206805 311372
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
  • 1 POUCH in 1 CARTON (67751-153-01) / 1 TABLET in 1 POUCH
source: ndc

Packages (1)

67751-153-01 1 POUCH in 1 CARTON (67751-153-01) / 1 TABLET in 1 POUCH

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": "f5db88bd-8ea6-0df0-e053-2995a90a18b4", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["206805", "311372"], "spl_set_id": ["219ab9c4-d0c4-4256-ab64-66d0260886bd"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-153-01)  / 1 TABLET in 1 POUCH", "package_ndc": "67751-153-01", "marketing_start_date": "20160917"}], "brand_name": "Claritin", "product_id": "67751-153_f5db88bd-8ea6-0df0-e053-2995a90a18b4", "dosage_form": "TABLET", "product_ndc": "67751-153", "generic_name": "LORATADINE", "labeler_name": "Navajo Manufacturing Company Inc.", "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": "20160917", "listing_expiration_date": "20261231"}