Package 0378-8880-10

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 0378-8880-10
Digits Only 0378888010
Product NDC 0378-8880
Description

1000 TABLET in 1 BOTTLE, PLASTIC (0378-8880-10)

Marketing

Marketing Status
Marketed Since 2011-06-01
Brand loratadine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1392dd15-842c-4689-87ba-caafc0503bca", "openfda": {"upc": ["0303788880100"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["3b307aea-5a68-4c82-959a-cda4ffbd0a4a"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0378-8880-10)", "package_ndc": "0378-8880-10", "marketing_start_date": "20110601"}], "brand_name": "Loratadine", "product_id": "0378-8880_1392dd15-842c-4689-87ba-caafc0503bca", "dosage_form": "TABLET", "product_ndc": "0378-8880", "generic_name": "loratadine", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076154", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}