Package 21130-780-03

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 21130-780-03
Digits Only 2113078003
Product NDC 21130-780
Product ID 21130-780_4650d218-040a-0b6e-e063-6294a90a887c
Description

30 TABLET in 1 BOTTLE (21130-780-03)

Marketing

Marketing Status
Marketed Since 2023-06-30
Brand loratadine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Loratadine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4650d218-040a-0b6e-e063-6294a90a887c", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["f2a2a754-0170-e37c-e053-2a95a90a4dca"], "manufacturer_name": ["Safeway, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (21130-780-03)", "package_ndc": "21130-780-03", "marketing_start_date": "20230630"}], "brand_name": "Loratadine", "product_id": "21130-780_4650d218-040a-0b6e-e063-6294a90a887c", "dosage_form": "TABLET", "product_ndc": "21130-780", "generic_name": "Loratadine", "labeler_name": "Safeway, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA210722", "marketing_category": "ANDA", "marketing_start_date": "20230630", "listing_expiration_date": "20261231"}