Package 16571-822-30
Brand: loratadine
Generic: loratadinePackage Facts
Identity
Package NDC
16571-822-30
Digits Only
1657182230
Product NDC
16571-822
Description
300 TABLET in 1 BOTTLE (16571-822-30)
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": "8b088034-c702-4b88-b4e3-421aa9739ec8", "openfda": {"upc": ["0316571822010", "0316571822034"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["d28128a3-af54-440e-9bd4-0fccf393d18a"], "manufacturer_name": ["Rising Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-822-01)", "package_ndc": "16571-822-01", "marketing_start_date": "20220310"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (16571-822-03)", "package_ndc": "16571-822-03", "marketing_start_date": "20220310"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (16571-822-30)", "package_ndc": "16571-822-30", "marketing_start_date": "20220310"}], "brand_name": "Loratadine", "product_id": "16571-822_8b088034-c702-4b88-b4e3-421aa9739ec8", "dosage_form": "TABLET", "product_ndc": "16571-822", "generic_name": "loratadine", "labeler_name": "Rising Pharmaceuticals, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA214684", "marketing_category": "ANDA", "marketing_start_date": "20220310", "listing_expiration_date": "20261231"}