70934-961 : Alfuzosin Hydrochloride Extended Release 10 mg Oral Tablet


NDC: 70934-961
Labeler: Denton Pharma, Inc. Dba Northwind Pharmaceuticals
Product Type: Human Prescription Drug
Drug Name:  Alfuzosin Hydrochloride Extended Release
Dosage Form: Oral Tablet
Application #: ANDA090284
Rev. Date: 


NDC Package Codes:

  • 70934-961-30: 30 TABLET IN 1 BOTTLE, PLASTIC (70934‑961‑30)

Active Ingredients:

  • Alfuzosin Hydrochloride

Dosage Strength:

  • 10 mg

Pharmaceutical Classes:

  • Adrenergic alpha-Antagonists [MoA]
  • alpha-Adrenergic Blocker [EPC]

Related Products:

Based on records with the same trade name.
  • 69097-844 Alfuzosin Hydrochloride Extended Release 10 mg Oral Tablet by Cipla USA Inc.
  • 69189-0304 Alfuzosin Hydrochloride Extended Release 10 mg Oral Tablet by Avera Mckennan Hospital

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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.