Package 71598-200-15

Brand: bupropidex

Generic: dextromethorphan hydrobromide
NDC Package

Package Facts

Identity

Package NDC 71598-200-15
Digits Only 7159820015
Product NDC 71598-200
Description

200 TABLET in 1 BOTTLE (71598-200-15)

Marketing

Marketing Status
Marketed Since 2023-12-01
Brand bupropidex
Generic dextromethorphan hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4081a7ee-5e35-6ad6-e063-6394a90a7047", "openfda": {"unii": ["9D2RTI9KYH"], "rxcui": ["2173733"], "spl_set_id": ["90cc9bcd-7891-4324-a1f4-f6df7a0457e0"], "manufacturer_name": ["DXM Pharmacuetical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (71598-200-15)", "package_ndc": "71598-200-15", "marketing_start_date": "20231201"}], "brand_name": "BupropiDex", "product_id": "71598-200_4081a7ee-5e35-6ad6-e063-6394a90a7047", "dosage_form": "TABLET", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "71598-200", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE", "labeler_name": "DXM Pharmacuetical, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BupropiDex", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}