Package 69367-253-30

Brand: triprolidine hydrochloride

Generic: triprolidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-253-30
Digits Only 6936725330
Product NDC 69367-253
Description

1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2020-03-09
Brand triprolidine hydrochloride
Generic triprolidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "63d97fa4-9b2d-4eef-8865-0cc4af5bc9e8", "openfda": {"upc": ["0369367253307"], "unii": ["YAN7R5L890"], "rxcui": ["1491649"], "spl_set_id": ["a9f01760-e335-4410-a9b8-8edce2841270"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (69367-253-30)  / 30 mL in 1 BOTTLE, DROPPER", "package_ndc": "69367-253-30", "marketing_start_date": "20200309"}], "brand_name": "TRIPROLIDINE HYDROCHLORIDE", "product_id": "69367-253_63d97fa4-9b2d-4eef-8865-0cc4af5bc9e8", "dosage_form": "SYRUP", "product_ndc": "69367-253", "generic_name": "TRIPROLIDINE HYDROCHLORIDE", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TRIPROLIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": ".938 mg/mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200309", "listing_expiration_date": "20261231"}