allegra-d

Generic: fexofenadine hydrochloride and pseudoephedrine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name allegra-d
Generic Name fexofenadine hydrochloride and pseudoephedrine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 60 mg/1, pseudoephedrine hydrochloride 120 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1203
Product ID 50090-1203_a0388348-fc41-4d13-81ad-d8f25cd154d9
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA020786
Listing Expiration 2026-12-31
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 500901203
Hyphenated Format 50090-1203

Supplemental Identifiers

RxCUI
997406 997512
UNII
2S068B75ZU 6V9V2RYJ8N

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 (source: ndc)
Generic Name fexofenadine hydrochloride and pseudoephedrine hydrochloride (source: ndc)
Application Number NDA020786 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 120 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-1203-0) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

50090-1203-0 1 BLISTER PACK in 1 CARTON (50090-1203-0) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

fexofenadine hydrochloride (60 mg/1) pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

ALLEGRA-D ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a0388348-fc41-4d13-81ad-d8f25cd154d9", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406", "997512"], "spl_set_id": ["705e1087-61cb-43c3-8675-f56626a1707b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-1203-0)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "50090-1203-0", "marketing_start_date": "20141128"}], "brand_name": "ALLEGRA-D", "product_id": "50090-1203_a0388348-fc41-4d13-81ad-d8f25cd154d9", "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": "50090-1203", "generic_name": "fexofenadine hydrochloride and pseudoephedrine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALLEGRA-D", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "NDA020786", "marketing_category": "NDA", "marketing_start_date": "20110303", "listing_expiration_date": "20261231"}