pseudoephedrine hydrochloride
Generic: pseudoephedrine hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
pseudoephedrine hydrochloride
Generic Name
pseudoephedrine hydrochloride
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
pseudoephedrine hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6727
Product ID
0904-6727_3c446d89-47d5-b29f-e063-6294a90a2386
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Marketing Start
2019-01-31
Marketing End
2026-12-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046727
Hyphenated Format
0904-6727
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
pseudoephedrine hydrochloride (source: ndc)
Generic Name
pseudoephedrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (0904-6727-60)
Packages (1)
Ingredients (1)
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"}