13672-054 : Betapace Af 80 mg/80mg Oral Tablet


NDC: 13672-054
Labeler: Skyepharma Production Sas
Product Type: Human Prescription Drug
Drug Name:  Betapace Af
Dosage Form: Oral Tablet
Application #: NDA021151
Rev. Date: 


NDC Package Codes:

  • 13672-054-00: 60 MG IN 1 BOTTLE (13672‑054‑00)

Active Ingredients:

  • Sotalol Hydrochloride

Dosage Strength:

  • 80 mg/80mg

Pharmaceutical Classes:

  • Antiarrhythmic [EPC]
  • Cardiac Rhythm Alteration [PE]
  • Adrenergic beta-Antagonists [MoA]

Related Products:

Based on records with the same trade name.
  • 13672-055 Betapace Af 120 mg/120mg Oral Tablet by Skyepharma Production Sas
  • 13672-056 Betapace Af 160 mg/160mg Oral Tablet by Skyepharma Production Sas
  • 50419-115 Betapace 80 mg Oral Tablet by Bayer Healthcare Pharmaceuticals Inc.
  • 50419-116 Betapace 160 mg Oral Tablet by Bayer Healthcare Pharmaceuticals Inc.
  • 50419-119 Betapace 120 mg Oral Tablet by Bayer Healthcare Pharmaceuticals Inc.
  • 70515-115 Betapace Af 80 mg Oral Tablet by Covis Pharma
  • 70515-116 Betapace Af 160 mg Oral Tablet by Covis Pharma
  • 70515-119 Betapace Af 120 mg Oral Tablet by Covis Pharma
  • 83107-008 Betapace Af 80 mg Oral Tablet by Legacy Pharma USA, Inc.
  • 83107-009 Betapace Af 120 mg Oral Tablet by Legacy Pharma USA, Inc.
  • 83107-010 Betapace Af 160 mg Oral Tablet by Legacy Pharma USA, Inc.

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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.