Package 0031-9302-01

Brand: robitussin direct cough

Generic: dextromethorphan hydrobromide
NDC Package

Package Facts

Identity

Package NDC 0031-9302-01
Digits Only 0031930201
Product NDC 0031-9302
Description

18 CAPSULE, LIQUID FILLED in 1 BOTTLE (0031-9302-01)

Marketing

Marketing Status
Marketed Since 2022-07-15
Brand robitussin direct cough
Generic dextromethorphan hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13f2a432-de15-26a7-e063-6294a90a43e6", "openfda": {"unii": ["9D2RTI9KYH"], "rxcui": ["1090487"], "spl_set_id": ["70c9556b-063a-4fb3-96f6-1d4ffa495ed4"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 CAPSULE, LIQUID FILLED in 1 BOTTLE (0031-9302-01)", "package_ndc": "0031-9302-01", "marketing_start_date": "20220715"}], "brand_name": "Robitussin Direct Cough", "product_id": "0031-9302_13f2a432-de15-26a7-e063-6294a90a43e6", "dosage_form": "CAPSULE, LIQUID FILLED", "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": "0031-9302", "generic_name": "dextromethorphan hydrobromide", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Robitussin Direct Cough", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220715", "listing_expiration_date": "20261231"}