0093-5213 : Hctz 12.5 mg / Moexipril Hydrochloride 7.5 mg Oral Tablet


NDC: 0093-5213
Labeler: Teva Pharmaceuticals USA Inc
Product Type: Human Prescription Drug
Drug Name: Moexipril Hydrochloride and Hydrochlorothiazide
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA076980
Rev. Date: 


Appearance:


Markings: 9;3;5213
Shapes:  Oval
Colors:  Yellow
Size (mm): 10
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.

9 3 5213: (0093-5213) Hctz 12.5 mg / Moexipril Hydrochloride 7.5 mg Oral Tablet by Teva Pharmaceuticals USA 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:

  • 0093-5213-01: 100 TABLET, FILM COATED IN 1 BOTTLE (0093‑5213‑01)

Active Ingredients:

  • Moexipril Hydrochloride
  • Hydrochlorothiazide

Dosage Strength:

  • 7.5 mg
  • 12.5 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Magnesium Stearate
  • Povidone K29/32
  • Sodium Bicarbonate
  • Polyethylene Glycol 3350
  • Polyvinyl Alcohol
  • Talc
  • Titanium Dioxide
  • Fd&c Yellow No. 5
  • Aluminum Oxide
  • Fd&c Yellow No. 6

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.
  • 0093-5214 Hctz 12.5 mg / Moexipril Hydrochloride 15 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-5215 Hctz 25 mg / Moexipril Hydrochloride 15 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0574-0133 Hctz 12.5 mg / Moexipril Hydrochloride 7.5 mg Oral Tablet by Paddock Laboratories, Inc.
  • 0574-0134 Hctz 12.5 mg / Moexipril Hydrochloride 15 mg Oral Tablet by Paddock Laboratories, Inc.
  • 0574-0135 Hctz 25 mg / Moexipril Hydrochloride 15 mg Oral Tablet by Paddock Laboratories, Inc.
  • 23155-035 Moexipril Hydrochloride and Hydrochlorothiazide Oral Tablet, Film Coated by Heritage Pharmaceuticals Inc.
  • 23155-036 Moexipril Hydrochloride and Hydrochlorothiazide Oral Tablet, Film Coated by Heritage Pharmaceuticals Inc.
  • 23155-037 Moexipril Hydrochloride and Hydrochlorothiazide Oral Tablet, Film Coated by Heritage Pharmaceuticals Inc.
  • 42291-576 Moexipril Hydrochloride and Hydrochlorothiazide Oral Tablet, Film Coated by Avkare, Inc.
  • 42291-577 Moexipril Hydrochloride and Hydrochlorothiazide Oral Tablet, Film Coated by Avkare, Inc.
  • 42291-578 Moexipril Hydrochloride and Hydrochlorothiazide Oral Tablet, Film Coated by Avkare, Inc.
  • 54868-3443 Hctz 25 mg / Moexipril Hydrochloride 15 mg Oral Tablet by Physicians Total Care, Inc.
  • 68462-205 Hctz 25 mg / Moexipril Hydrochloride 15 mg Oral Tablet by Glenmark Generics Inc., USA
  • 68462-206 Hctz 12.5 mg / Moexipril Hydrochloride 15 mg Oral Tablet by Glenmark Generics Inc., USA
  • 68462-207 Hctz 12.5 mg / Moexipril Hydrochloride 7.5 mg Oral Tablet by Glenmark Generics Inc., USA

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 0093-5213 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.