11822-0021 : Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release


NDC: 11822-0021
Labeler: Rite Aid Corporation
Product Type: Human OTC Drug
Drug Name:  Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA215434
Rev. Date: 


NDC Package Codes:

  • 11822-0021-4: 4 BLISTER PACK IN 1 CARTON (11822‑0021‑4) / 5 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
  • 11822-0021-6: 6 BLISTER PACK IN 1 CARTON (11822‑0021‑6) / 5 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK

Active Ingredients:

  • Fexofenadine Hydrochloride
  • Pseudoephedrine Hydrochloride

Dosage Strength:

  • 60 mg
  • 120 mg

Pharmaceutical Classes:

  • Adrenergic alpha-Agonists [MoA]
  • Histamine H1 Receptor Antagonists [MoA]
  • Histamine-1 Receptor Antagonist [EPC]
  • alpha-Adrenergic Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0363-0044 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Walgreens Company
  • 0363-0094 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Walgreen Co.
  • 0363-2110 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Walgreens
  • 0536-1384 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Rugby Laboratories
  • 0536-1431 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Rugby Laboratories
  • 0555-0725 Fexofenadine Hydrochloride 60 mg / Pseudoephedrine Hydrochloride 120 mg 12 Hr Extended Release Tablet by Barr Laboratories Inc.
  • 21695-820 Fexofenadine Hydrochloride 60 mg / Pseudoephedrine Hydrochloride 120 mg 12 Hr Extended Release Tablet by Rebel Distributors Corp
  • 30142-059 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Kroger Company
  • 30142-097 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Kroger Company
  • 37808-999 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by H E B
  • 41415-995 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Publix Super Markets, Inc
  • 46122-452 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Amerisource Bergen
  • 46122-694 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Amerisource Bergen
  • 47335-724 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Sun Pharma Global Fze
  • 51316-007 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Cvs Pharmacy, Inc.
  • 51316-015 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Cvs Health Corp
  • 51660-037 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Ohm Laboratories Inc.
  • 54868-6087 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride (Fexofenadine Hydrochloride 60 mg / Pseudoephedrine Hydrochloride 120 mg) by Physicians Total Care, Inc.
  • 56062-999 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Publix Super Markets Inc
  • 58602-807 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Aurohealth LLC
  • More related products ...

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.