Package 46122-383-22

Brand: loratadine and pseudoephedrine

Generic: loratadine and pseudoephedrine
NDC Package

Package Facts

Identity

Package NDC 46122-383-22
Digits Only 4612238322
Product NDC 46122-383
Description

15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (46122-383-22)

Marketing

Marketing Status
Marketed Since 2017-08-02
Brand loratadine and pseudoephedrine
Generic loratadine and pseudoephedrine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39ace1fb-0f76-4ff6-8846-e6316ee972e5", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["96635cb0-8c78-4c3a-8294-2804ff26f90a"], "manufacturer_name": ["AMERISOURCE BERGEN"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (46122-383-22)", "package_ndc": "46122-383-22", "marketing_start_date": "20170802"}], "brand_name": "Loratadine and Pseudoephedrine", "product_id": "46122-383_39ace1fb-0f76-4ff6-8846-e6316ee972e5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "46122-383", "generic_name": "loratadine and pseudoephedrine", "labeler_name": "AMERISOURCE BERGEN", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine and Pseudoephedrine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}, {"name": "PSEUDOEPHEDRINE SULFATE", "strength": "240 mg/1"}], "application_number": "ANDA076557", "marketing_category": "ANDA", "marketing_start_date": "20170802", "listing_expiration_date": "20261231"}