25000-220 : Cetirizine Hydrochloride Tablets, 10 mg Tablets, 10 mg 10 mg Oral Tablet


NDC25000-220
Labeler: Marksans Pharma Limited
Product Type: Human OTC Drug
Drug Name:  Cetirizine Hydrochloride Tablets, 10 mg
Dosage Form: Oral Tablet
Application #: ANDA078933
Rev. Date: 


NDC Package Codes:

  • 25000-220-03: 1 BOTTLE IN 1 CARTON (25000‑220‑03) > 30 TABLET IN 1 BOTTLE
  • 25000-220-08: 1 BOTTLE IN 1 CARTON (25000‑220‑08) > 100 TABLET IN 1 BOTTLE
  • 25000-220-14: 1000 TABLET IN 1 BOTTLE (25000‑220‑14)
  • 25000-220-78: 1 BLISTER PACK IN 1 CARTON (25000‑220‑78) / 7 TABLET IN 1 BLISTER PACK
  • 25000-220-81: 1 BLISTER PACK IN 1 CARTON (25000‑220‑81) / 14 TABLET IN 1 BLISTER PACK

Active Ingredients:

  • Cetirizine Hydrochloride

Dosage Strength:

  • 10 mg

Pharmaceutical Classes:

  • Histamine H1 Receptor Antagonists [MoA]
  • Histamine-1 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 49483-692 Cetirizine Hydrochloride Tablets,10 mg Tablets,10 mg 10 mg Oral Tablet by Time Cap Laboratories, Inc.
  • 51655-842 Cetirizine Hydrochloride Tablets,10 mg Tablets,10 mg 10 mg Oral Tablet by Northwind Pharmaceuticals, LLC

NDC QR Code

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NDC 25000-220 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.