62135-701 : Amoxapine 50 mg Oral Tablet


NDC: 62135-701
Labeler: Chartwell Rx, LLC
Product Type: Human Prescription Drug
Drug Name:  Amoxapine
Dosage Form: Oral Tablet
Application #: ANDA072944
Rev. Date: 


NDC Package Codes:

  • 62135-701-90: 90 TABLET IN 1 BOTTLE (62135‑701‑90)

Active Ingredients:

  • Amoxapine

Dosage Strength:

  • 50 mg

Pharmaceutical Classes:

  • Tricyclic Antidepressant [EPC]

Related Products:

Based on records with the same trade name.
  • 62135-700 Amoxapine 25 mg Oral Tablet by Chartwell Rx, LLC
  • 62135-702 Amoxapine 100 mg Oral Tablet by Chartwell Rx, LLC
  • 62135-703 Amoxapine 150 mg Oral Tablet by Chartwell Rx, LLC
  • 0591-5713 Amoxapine 25 mg Oral Tablet by Watson Laboratories, Inc.
  • 0591-5714 Amoxapine 50 mg Oral Tablet by Watson Laboratories, Inc.
  • 0591-5715 Amoxapine 100 mg Oral Tablet by Watson Laboratories, Inc.
  • 0591-5716 Amoxapine 150 mg Oral Tablet by Watson Laboratories, Inc.
  • 54868-2438 Amoxapine 50 mg Oral Tablet by Physicians Total Care, 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.