60687-175 : Fexofenadine 180 mg Oral Tablet, Film Coated


NDC: 60687-175
Labeler: American Health Packaging
Product Type: Human OTC Drug
Drug Name:  Fexofenadine
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA079112
Rev. Date: 


NDC Package Codes:

  • 60687-175-01: 100 BLISTER PACK IN 1 BOX, UNIT‑DOSE (60687‑175‑01) > 1 TABLET, FILM COATED IN 1 BLISTER PACK (60687‑175‑11)

Active Ingredients:

  • Fexofenadine Hydrochloride

Dosage Strength:

  • 180 mg

Related Products:

Based on records with the same trade name.
  • 42507-425 Fexofenadine Hydrochloride 60 mg Oral Tablet by Hyvee Inc
  • 55648-744 Fexofenadine Hydrochloride 30 mg Oral Tablet by Wockhardt Limited
  • 55648-982 Fexofenadine Hydrochloride 60 mg Oral Tablet by Wockhardt Limited
  • 55648-987 Fexofenadine Hydrochloride 180 mg Oral Tablet by Wockhardt Limited
  • 64679-744 Fexofenadine Hydrochloride 30 mg Oral Tablet by Wockhardt USA LLC.
  • 64679-982 Fexofenadine Hydrochloride 60 mg Oral Tablet by Wockhardt USA LLC.
  • 64679-987 Fexofenadine Hydrochloride 180 mg Oral Tablet by Wockhardt USA LLC.
  • 72189-305 Fexofenadine 180 mg Oral Tablet by Directrx

NDC QR Code

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