Package 17856-0557-1
Brand: Loratadine
Generic: LoratadinePackage Facts
Identity
Package NDC
17856-0557-1
Digits Only
1785605571
Product NDC
17856-0557
Description
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0557-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0557-2)
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": "34f57090-88ba-723c-e063-6294a90a36d4", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["692783"], "spl_set_id": ["999a1080-5bbd-4027-b6e7-a90a6941ee27"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0557-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0557-2)", "package_ndc": "17856-0557-1", "marketing_start_date": "20240514"}], "brand_name": "Loratadine", "product_id": "17856-0557_34f57090-88ba-723c-e063-6294a90a36d4", "dosage_form": "SOLUTION", "product_ndc": "17856-0557", "generic_name": "Loratadine", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/5mL"}], "application_number": "ANDA077421", "marketing_category": "ANDA", "marketing_start_date": "20190213", "listing_expiration_date": "20261231"}