nasal decongestant

Generic: pseudoephedrine hcl

Labeler: l.n.k. international, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name nasal decongestant
Generic Name pseudoephedrine hcl
Labeler l.n.k. international, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

pseudoephedrine hydrochloride 30 mg/1

Manufacturer
L.N.K. International, Inc.

Identifiers & Regulatory

Product NDC 50844-112
Product ID 50844-112_962e4e53-1137-48a6-888c-05bb0b5e648b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 1981-08-25

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50844112
Hyphenated Format 50844-112

Supplemental Identifiers

RxCUI
1049160
UPC
0050844112223
UNII
6V9V2RYJ8N

Packaging Origin

Original Packager
true

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 nasal decongestant (source: ndc)
Generic Name pseudoephedrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (50844-112-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (50844-112-22) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • 8 BLISTER PACK in 1 CARTON (50844-112-46) / 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (3)

50844-112-08 2 BLISTER PACK in 1 CARTON (50844-112-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK 50844-112-22 4 BLISTER PACK in 1 CARTON (50844-112-22) / 12 TABLET, FILM COATED in 1 BLISTER PACK 50844-112-46 8 BLISTER PACK in 1 CARTON (50844-112-46) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

pseudoephedrine hydrochloride (30 mg/1)

Linked Drug Pages (1)

Nasal Decongestant ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "962e4e53-1137-48a6-888c-05bb0b5e648b", "openfda": {"upc": ["0050844112223"], "unii": ["6V9V2RYJ8N"], "rxcui": ["1049160"], "spl_set_id": ["f12b7f07-0b81-4cab-ae0f-43a7bf9b4bc5"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50844-112-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-112-08", "marketing_start_date": "19810825"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (50844-112-22)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-112-22", "marketing_start_date": "19810825"}, {"sample": false, "description": "8 BLISTER PACK in 1 CARTON (50844-112-46)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-112-46", "marketing_start_date": "19810825"}], "brand_name": "Nasal Decongestant", "product_id": "50844-112_962e4e53-1137-48a6-888c-05bb0b5e648b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "50844-112", "generic_name": "Pseudoephedrine HCl", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Decongestant", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19810825", "listing_expiration_date": "20261231"}