claritin

Generic: loratadine

Labeler: select consumer group
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name claritin
Generic Name loratadine
Labeler select consumer group
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Select Consumer Group

Identifiers & Regulatory

Product NDC 85237-1630
Product ID 85237-1630_46fe1007-0c18-a3ba-e063-6394a90a7b11
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075209
Listing Expiration 2026-12-31
Marketing Start 2020-12-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 852371630
Hyphenated Format 85237-1630

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 ANDA075209 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (85237-1630-1) / 1 TABLET in 1 BLISTER PACK
  • 20 POUCH in 1 BOX, UNIT-DOSE (85237-1630-3) / 1 TABLET in 1 POUCH
  • 25 POUCH in 1 BOX, UNIT-DOSE (85237-1630-4) / 1 TABLET in 1 POUCH
source: ndc

Packages (3)

85237-1630-1 1 BLISTER PACK in 1 CARTON (85237-1630-1) / 1 TABLET in 1 BLISTER PACK 85237-1630-3 20 POUCH in 1 BOX, UNIT-DOSE (85237-1630-3) / 1 TABLET in 1 POUCH 85237-1630-4 25 POUCH in 1 BOX, UNIT-DOSE (85237-1630-4) / 1 TABLET in 1 POUCH

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Claritin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46fe1007-0c18-a3ba-e063-6394a90a7b11", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["206805", "311372"], "spl_set_id": ["3c9ad1f8-e8ef-bcd0-e063-6394a90ac20e"], "manufacturer_name": ["Select Consumer Group"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (85237-1630-1)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "85237-1630-1", "marketing_start_date": "20250818"}, {"sample": false, "description": "20 POUCH in 1 BOX, UNIT-DOSE (85237-1630-3)  / 1 TABLET in 1 POUCH", "package_ndc": "85237-1630-3", "marketing_start_date": "20251227"}, {"sample": false, "description": "25 POUCH in 1 BOX, UNIT-DOSE (85237-1630-4)  / 1 TABLET in 1 POUCH", "package_ndc": "85237-1630-4", "marketing_start_date": "20251227"}], "brand_name": "Claritin", "product_id": "85237-1630_46fe1007-0c18-a3ba-e063-6394a90a7b11", "dosage_form": "TABLET", "product_ndc": "85237-1630", "generic_name": "loratadine", "labeler_name": "Select Consumer Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Claritin", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA075209", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}