Package 0904-6727-60

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6727-60
Digits Only 0904672760
Product NDC 0904-6727
Description

100 TABLET in 1 BOTTLE (0904-6727-60)

Marketing

Marketing Status
Discontinued 2026-12-31
Brand pseudoephedrine hydrochloride
Generic pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c446d89-47d5-b29f-e063-6294a90a2386", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049160"], "spl_set_id": ["78faa497-6743-b85b-e053-2a91aa0ae822"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0904-6727-60)", "package_ndc": "0904-6727-60", "marketing_end_date": "20261231", "marketing_start_date": "20190131"}], "brand_name": "Pseudoephedrine Hydrochloride", "product_id": "0904-6727_3c446d89-47d5-b29f-e063-6294a90a2386", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0904-6727", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20190131"}