Package 28595-802-08

Brand: histex

Generic: triprolidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 28595-802-08
Digits Only 2859580208
Product NDC 28595-802
Product ID 28595-802_0e764061-e7a9-6701-e063-6394a90a489f
Description

237 mL in 1 BOTTLE (28595-802-08)

Marketing

Marketing Status
Marketed Since 2014-03-04
Brand histex
Generic triprolidine hydrochloride
Sample Package No

Linked Drug Pages (1)

HISTEX ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e764061-e7a9-6701-e063-6394a90a489f", "openfda": {"unii": ["YAN7R5L890"], "rxcui": ["1490671"], "spl_set_id": ["cc466d33-cf3e-4f1c-a794-6d3d79903adf"], "manufacturer_name": ["Allegis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (28595-802-08)", "package_ndc": "28595-802-08", "marketing_start_date": "20140304"}], "brand_name": "HISTEX", "product_id": "28595-802_0e764061-e7a9-6701-e063-6394a90a489f", "dosage_form": "SYRUP", "product_ndc": "28595-802", "generic_name": "TRIPROLIDINE HYDROCHLORIDE", "labeler_name": "Allegis Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HISTEX", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "2.5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140304", "listing_expiration_date": "20261231"}