Package 0363-0752-30

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 0363-0752-30
Digits Only 0363075230
Product NDC 0363-0752
Description

3 BLISTER PACK in 1 CARTON (0363-0752-30) / 10 TABLET, CHEWABLE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-07-26
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": "2a760d97-9a3c-7ae0-e063-6394a90a4644", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["665078"], "spl_set_id": ["645c26ab-08ab-4a69-ae7d-7802d8ec5922"], "manufacturer_name": ["WALGREEN COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0363-0752-30)  / 10 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0363-0752-30", "marketing_start_date": "20190726"}], "brand_name": "Loratadine", "product_id": "0363-0752_2a760d97-9a3c-7ae0-e063-6394a90a4644", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0363-0752", "generic_name": "Loratadine", "labeler_name": "WALGREEN COMPANY", "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": "20190726", "listing_expiration_date": "20261231"}