nasal decongestant d

Generic: pseudoephedrine hydrochloride

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nasal decongestant d
Generic Name pseudoephedrine hydrochloride
Labeler walgreen company
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

pseudoephedrine hydrochloride 120 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-3301
Product ID 0363-3301_0c060566-54b0-4fd9-9040-a7cc8917909d
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075153
Listing Expiration 2026-12-31
Marketing Start 2022-04-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03633301
Hyphenated Format 0363-3301

Supplemental Identifiers

RxCUI
1049154
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 d (source: ndc)
Generic Name pseudoephedrine hydrochloride (source: ndc)
Application Number ANDA075153 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (0363-3301-52) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
  • 20 BLISTER PACK in 1 CARTON (0363-3301-60) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

0363-3301-52 10 BLISTER PACK in 1 CARTON (0363-3301-52) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK 0363-3301-60 20 BLISTER PACK in 1 CARTON (0363-3301-60) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (1)

pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

Nasal Decongestant D ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0c060566-54b0-4fd9-9040-a7cc8917909d", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["9572b6c9-172b-459e-82d1-7f92f0eaec8e"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (0363-3301-52)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-3301-52", "marketing_start_date": "20220406"}, {"sample": false, "description": "20 BLISTER PACK in 1 CARTON (0363-3301-60)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-3301-60", "marketing_start_date": "20220406"}], "brand_name": "Nasal Decongestant D", "product_id": "0363-3301_0c060566-54b0-4fd9-9040-a7cc8917909d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0363-3301", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Decongestant D", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA075153", "marketing_category": "ANDA", "marketing_start_date": "20220406", "listing_expiration_date": "20261231"}