62135-967 : Moexipril Hydrochloride 7.5 mg Oral Tablet, Film Coated


NDC: 62135-967
Labeler: Chartwell Rx, LLC
Product Type: Human Prescription Drug
Drug Name:  Moexipril Hydrochloride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA077536
Rev. Date: 


NDC Package Codes:

  • 62135-967-90: 90 TABLET, FILM COATED IN 1 BOTTLE (62135‑967‑90)

Active Ingredients:

  • Moexipril Hydrochloride

Dosage Strength:

  • 7.5 mg

Pharmaceutical Classes:

  • Angiotensin Converting Enzyme Inhibitor [EPC]
  • Angiotensin-converting Enzyme Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 62135-969 Moexipril Hydrochloride 15 mg Oral Tablet, Film Coated by Chartwell Rx, LLC
  • 0093-0017 Moexipril Hydrochloride 7.5 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-5150 Moexipril Hydrochloride 15 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0574-0110 Moexipril Hydrochloride 7.5 mg Oral Tablet by Paddock Laboratories, Inc.
  • 0574-0112 Moexipril Hydrochloride 15 mg Oral Tablet by Paddock Laboratories, Inc.
  • 54868-4883 Moexipril Hydrochloride 15 mg Oral Tablet by Physicians Total Care, Inc.
  • 54868-5928 Moexipril Hydrochloride 7.5 mg Oral Tablet by Physicians Total Care, Inc.
  • 60505-0271 Moexipril Hydrochloride 7.5 mg Oral Tablet by Apotex Corp.
  • 60505-0272 Moexipril Hydrochloride 15 mg Oral Tablet by Apotex Corp.
  • 68151-1472 Moexipril Hydrochloride 7.5 mg Oral Tablet, Film Coated by Carilion Materials Management
  • 68151-1473 Moexipril Hydrochloride 15 mg Oral Tablet, Film Coated by Carilion Materials Management
  • 68462-208 Moexipril Hydrochloride 15 mg Oral Tablet by Glenmark Generics Inc., USA
  • 68462-209 Moexipril Hydrochloride 7.5 mg Oral Tablet by Glenmark Generics Inc., USA
  • 69189-0325 Moexipril Hydrochloride 7.5 mg Oral Tablet, Film Coated by Avera Mckennan Hospital

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Related Discussions:

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