allegra-d allergy and congestion

Generic: fexofenadine hydrochloride and pseudoephedrine hydrochloride

Labeler: chattem, inc.
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name allegra-d allergy and congestion
Generic Name fexofenadine hydrochloride and pseudoephedrine hydrochloride
Labeler chattem, inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1, pseudoephedrine hydrochloride 240 mg/1

Manufacturer
Chattem, Inc.

Identifiers & Regulatory

Product NDC 41167-4320
Product ID 41167-4320_de126d31-d1bb-490f-bf3f-fd9faf4f20ab
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA021704
Listing Expiration 2027-12-31
Marketing Start 2011-03-03

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 411674320
Hyphenated Format 41167-4320

Supplemental Identifiers

RxCUI
997415 997515
UNII
2S068B75ZU 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 allegra-d allergy and congestion (source: ndc)
Generic Name fexofenadine hydrochloride and pseudoephedrine hydrochloride (source: ndc)
Application Number NDA021704 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
  • 240 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (41167-4320-5) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (41167-4320-7) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (2)

fexofenadine hydrochloride (180 mg/1) pseudoephedrine hydrochloride (240 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "de126d31-d1bb-490f-bf3f-fd9faf4f20ab", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997415", "997515"], "spl_set_id": ["1fb77d6a-fae2-40ae-8f8e-fa2dc66f4403"], "manufacturer_name": ["Chattem, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (41167-4320-5)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "41167-4320-5", "marketing_start_date": "20110303"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (41167-4320-7)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "41167-4320-7", "marketing_start_date": "20110303"}], "brand_name": "Allegra-D Allergy and Congestion", "product_id": "41167-4320_de126d31-d1bb-490f-bf3f-fd9faf4f20ab", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "41167-4320", "generic_name": "fexofenadine hydrochloride and pseudoephedrine hydrochloride", "labeler_name": "Chattem, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allegra-D Allergy and Congestion", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "NDA021704", "marketing_category": "NDA", "marketing_start_date": "20110303", "listing_expiration_date": "20271231"}