Package 53345-052-01

Brand: asp daytime pe

Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53345-052-01
Digits Only 5334505201
Product NDC 53345-052
Product ID 53345-052_27c81691-e7ca-70c6-e063-6394a90a4888
Description

1 BAG in 1 BOX (53345-052-01) / 4000 CAPSULE, LIQUID FILLED in 1 BAG

Marketing

Marketing Status
Marketed Since 2020-08-01
Brand asp daytime pe
Generic acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

ASP Daytime PE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "27c81691-e7ca-70c6-e063-6394a90a4888", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["b84f2392-0b24-4af0-80f7-c45454093f51"], "manufacturer_name": ["Humanwell PuraCap Pharmaceutical (Wuhan), Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 BOX (53345-052-01)  / 4000 CAPSULE, LIQUID FILLED in 1 BAG", "package_ndc": "53345-052-01", "marketing_start_date": "20200801"}], "brand_name": "ASP Daytime PE", "product_id": "53345-052_27c81691-e7ca-70c6-e063-6394a90a4888", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "53345-052", "generic_name": "acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride", "labeler_name": "Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ASP Daytime PE", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}