69238-2026 : Amlodipine 1 mg/ml Oral Suspension


NDC: 69238-2026
Labeler: Amneal Pharmaceuticals Ny LLC
Product Type: Human Prescription Drug
Drug Name:  Amlodipine
Dosage Form: Oral Suspension
Application #: ANDA215035
Rev. Date: 


NDC Package Codes:

  • 69238-2026-7: 1 BOTTLE IN 1 CARTON (69238‑2026‑7) / 150 ML IN 1 BOTTLE

Active Ingredients:

  • Amlodipine Benzoate

Dosage Strength:

  • 1 mg/mL

Pharmaceutical Classes:

  • Calcium Channel Antagonists [MoA]
  • Calcium Channel Blocker [EPC]
  • Cytochrome P450 3A Inhibitors [MoA]
  • Dihydropyridine Calcium Channel Blocker [EPC]
  • Dihydropyridines [CS]

Related Products:

Based on records with the same trade name.
  • 33342-015 Amlodipine (As Amlodipine Besylate) 5 mg Oral Tablet by Macleods Pharmaceuticals Limited
  • 33342-016 Amlodipine (As Amlodipine Besylate) 10 mg Oral Tablet by Macleods Pharmaceuticals Limited
  • 49349-160 Amlodipine (As Amlodipine Besylate) 10 mg Oral Tablet by Remedyrepack Inc.
  • 53808-0686 Amlodipine 10 mg Oral Tablet by State of Florida Doh Central Pharmacy
  • 57664-568 Amlodipine (As Amlodipine Besylate) 2.5 mg Oral Tablet by Caraco Pharmaceutical Laboratories, Ltd.
  • 57664-569 Amlodipine (As Amlodipine Besylate) 5 mg Oral Tablet by Caraco Pharmaceutical Laboratories, Ltd.
  • 57664-570 Amlodipine (As Amlodipine Besylate) 10 mg Oral Tablet by Caraco Pharmaceutical Laboratories, Ltd.

NDC 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.