Package 71610-423-60
Brand: loratadine
Generic: loratadinePackage Facts
Identity
Package NDC
71610-423-60
Digits Only
7161042360
Product NDC
71610-423
Description
90 TABLET in 1 BOTTLE (71610-423-60)
Marketing
Marketing Status
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": "c1e2a0e1-48b7-4481-8ed8-3197bf7d05a2", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["8ffe2faf-3253-4121-a069-6f46e319c6f0"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-423-60)", "package_ndc": "71610-423-60", "marketing_start_date": "20200501"}], "brand_name": "Loratadine", "product_id": "71610-423_c1e2a0e1-48b7-4481-8ed8-3197bf7d05a2", "dosage_form": "TABLET", "product_ndc": "71610-423", "generic_name": "Loratadine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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": "20181206", "listing_expiration_date": "20261231"}