loratadine

Generic: loratadine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2551
Product ID 71335-2551_99fa3280-671d-46b4-8b66-94b9171c9ad7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211718
Listing Expiration 2026-12-31
Marketing Start 2023-07-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352551
Hyphenated Format 71335-2551

Supplemental Identifiers

RxCUI
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 loratadine (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA211718 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (71335-2551-1)
  • 30 TABLET in 1 BOTTLE (71335-2551-2)
  • 60 TABLET in 1 BOTTLE (71335-2551-3)
  • 14 TABLET in 1 BOTTLE (71335-2551-4)
  • 10 TABLET in 1 BOTTLE (71335-2551-5)
  • 90 TABLET in 1 BOTTLE (71335-2551-6)
  • 28 TABLET in 1 BOTTLE (71335-2551-7)
  • 15 TABLET in 1 BOTTLE (71335-2551-8)
  • 100 TABLET in 1 BOTTLE (71335-2551-9)
source: ndc

Packages (9)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99fa3280-671d-46b4-8b66-94b9171c9ad7", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["7f97595b-9df7-4834-82f0-5e4ce329c118"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2551-1)", "package_ndc": "71335-2551-1", "marketing_start_date": "20250121"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2551-2)", "package_ndc": "71335-2551-2", "marketing_start_date": "20250121"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2551-3)", "package_ndc": "71335-2551-3", "marketing_start_date": "20250121"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-2551-4)", "package_ndc": "71335-2551-4", "marketing_start_date": "20250121"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2551-5)", "package_ndc": "71335-2551-5", "marketing_start_date": "20250121"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2551-6)", "package_ndc": "71335-2551-6", "marketing_start_date": "20250121"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2551-7)", "package_ndc": "71335-2551-7", "marketing_start_date": "20250121"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-2551-8)", "package_ndc": "71335-2551-8", "marketing_start_date": "20250121"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2551-9)", "package_ndc": "71335-2551-9", "marketing_start_date": "20250121"}], "brand_name": "Loratadine", "product_id": "71335-2551_99fa3280-671d-46b4-8b66-94b9171c9ad7", "dosage_form": "TABLET", "product_ndc": "71335-2551", "generic_name": "Loratadine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA211718", "marketing_category": "ANDA", "marketing_start_date": "20230728", "listing_expiration_date": "20261231"}