72789-371 : Telmisartan 20 mg Oral Tablet


NDC: 72789-371
Labeler: Pd-rx Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Telmisartan
Dosage Form: Oral Tablet
Application #: ANDA205150
Rev. Date: 


NDC Package Codes:

  • 72789-371-90: 90 TABLET IN 1 BOTTLE, PLASTIC (72789‑371‑90)

Active Ingredients:

  • Telmisartan

Dosage Strength:

  • 20 mg

Pharmaceutical Classes:

  • Angiotensin 2 Receptor Antagonists [MoA]
  • Angiotensin 2 Receptor Blocker [EPC]

Related Products:

Based on records with the same trade name.
  • 0054-0542 Telmisartan 20 mg/1 Oral Tablet by Roxane Laboratories, Inc.
  • 0054-0543 Telmisartan 40 mg/1 Oral Tablet by Roxane Laboratories, Inc.
  • 0054-0544 Telmisartan 80 mg/1 Oral Tablet by Roxane Laboratories, Inc.
  • 0378-2920 Telmisartan 20 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 0378-2921 Telmisartan 40 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 0378-2922 Telmisartan 80 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 0591-3292 Telmisartan 20 mg/1 Oral Tablet by Watson Laboratories, Inc.
  • 0591-3293 Telmisartan 40 mg/1 Oral Tablet by Watson Laboratories, Inc.
  • 0591-3294 Telmisartan 80 mg/1 Oral Tablet by Watson Laboratories, Inc.
  • 0603-5914 Telmisartan 20 mg Oral Tablet by Qualitest Pharmaceuticals
  • 0603-5915 Telmisartan 40 mg Oral Tablet by Qualitest Pharmaceuticals
  • 0603-5916 Telmisartan 80 mg Oral Tablet by Qualitest Pharmaceuticals
  • 0781-5372 Telmisartan 20 mg Oral Tablet by Sandoz Inc
  • 0781-5374 Telmisartan 40 mg Oral Tablet by Sandoz Inc
  • 0781-5378 Telmisartan 80 mg Oral Tablet by Sandoz Inc
  • 13668-156 Telmisartan 20 mg Oral Tablet by Torrent Pharmaceuticals Limited
  • 13668-157 Telmisartan 40 mg Oral Tablet by Torrent Pharmaceuticals Limited
  • 13668-158 Telmisartan 80 mg Oral Tablet by Torrent Pharmaceuticals Limited
  • 31722-802 Telmisartan 20 mg Oral Tablet by Camber Pharmaceuticals, Inc.
  • 31722-803 Telmisartan 40 mg Oral Tablet by Camber Pharmaceuticals, Inc.
  • More related products ...

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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.