loratadine

Generic: loratadine

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6852
Product ID 0904-6852_7c3836c3-7476-49b8-ac03-11718d17c813
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076301
Listing Expiration 2026-12-31
Marketing Start 2005-02-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046852
Hyphenated Format 0904-6852

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 ANDA076301 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0904-6852-72) / 300 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0904-6852-89) / 90 TABLET in 1 BOTTLE
source: ndc

Packages (2)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c3836c3-7476-49b8-ac03-11718d17c813", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["dee25423-377b-4b94-a4a8-0dfb8f51aaab"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6852-72)  / 300 TABLET in 1 BOTTLE", "package_ndc": "0904-6852-72", "marketing_start_date": "20190604"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6852-89)  / 90 TABLET in 1 BOTTLE", "package_ndc": "0904-6852-89", "marketing_start_date": "20190408"}], "brand_name": "Loratadine", "product_id": "0904-6852_7c3836c3-7476-49b8-ac03-11718d17c813", "dosage_form": "TABLET", "product_ndc": "0904-6852", "generic_name": "Loratadine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076301", "marketing_category": "ANDA", "marketing_start_date": "20050221", "listing_expiration_date": "20261231"}