Package 51079-246-20

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 51079-246-20
Digits Only 5107924620
Product NDC 51079-246
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-246-20) / 1 TABLET in 1 BLISTER PACK (51079-246-01)

Marketing

Marketing Status
Marketed Since 2013-04-30
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": "3a865b90-4189-3e83-e063-6394a90aba53", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["1fc9ddd1-393d-4fe2-a9e0-d192df7331db"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-246-20)  / 1 TABLET in 1 BLISTER PACK (51079-246-01)", "package_ndc": "51079-246-20", "marketing_start_date": "20130430"}], "brand_name": "Loratadine", "product_id": "51079-246_3a865b90-4189-3e83-e063-6394a90aba53", "dosage_form": "TABLET", "product_ndc": "51079-246", "generic_name": "loratadine", "labeler_name": "Mylan Institutional 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": "20130430", "listing_expiration_date": "20261231"}