0091-3720 : Uniretic 15/12.5 Oral Tablet


NDC: 0091-3720
Labeler: Ucb, Inc.
Product Type: Human Prescription Drug
Drug Name:  Uniretic
Dosage Form: Oral Tablet, Film Coated
Application #: NDA020729
Rev. Date: 


Appearance:


Markings: 720;S;P
Shapes:  Oval
Colors:  White
Size (mm): 12
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

720 S P: (0091-3720) Uniretic 15/12.5 Oral Tablet by Ucb, Inc.
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 0091-3720-01: 100 TABLET, FILM COATED IN 1 BOTTLE (0091‑3720‑01)

Active Ingredients:

  • Hydrochlorothiazide
  • Moexipril Hydrochloride

Dosage Strength:

  • 12.5 mg
  • 15 mg

Inactive Ingredients:

  • Lactose
  • Magnesium Oxide
  • Crospovidone
  • Magnesium Stearate
  • Gelatin
  • Hydroxypropyl Cellulose (Type H)
  • Hypromelloses
  • Polyethylene Glycol 6000
  • Titanium Dioxide

Pharmaceutical Classes:

  • Angiotensin Converting Enzyme Inhibitor [EPC]
  • Angiotensin-converting Enzyme Inhibitors [MoA]
  • Increased Diuresis [PE]
  • Thiazide Diuretic [EPC]
  • Thiazides [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 0091-3712 Uniretic 7.5/12.5 Oral Tablet by Ucb, Inc.
  • 0091-3725 Uniretic 15/25 (Moexipril Hydrochloride / Hctz) Oral Tablet by Ucb, Inc.

NDC QR Code

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NDC 0091-3720 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.