Package 51660-753-31

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 51660-753-31
Digits Only 5166075331
Product NDC 51660-753
Product ID 51660-753_48a60b3d-d011-4d0f-84dc-414c713c76ba
Description

3 BLISTER PACK in 1 CARTON (51660-753-31) / 10 TABLET, CHEWABLE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-06-01
Brand loratadine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Loratadine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48a60b3d-d011-4d0f-84dc-414c713c76ba", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["665078"], "spl_set_id": ["b83de07d-37f4-42b4-b43e-29173454bef0"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (51660-753-31)  / 10 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "51660-753-31", "marketing_start_date": "20180601"}], "brand_name": "Loratadine", "product_id": "51660-753_48a60b3d-d011-4d0f-84dc-414c713c76ba", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "51660-753", "generic_name": "Loratadine", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/1"}], "application_number": "ANDA210088", "marketing_category": "ANDA", "marketing_start_date": "20180601", "listing_expiration_date": "20261231"}