62175-362 : Monoket 20 mg Oral Tablet


NDC: 62175-362
Labeler: Kremers Urban Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Monoket
Dosage Form: Oral Tablet
Application #: NDA020215
Rev. Date: 


Appearance:


Markings: 20;SCHWARZ;620
Shapes:  Round
Colors:  White
Size (mm): 9
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.

NDC Package Codes:

  • 62175-362-01: 100 TABLET IN 1 BOTTLE (62175‑362‑01)

Active Ingredients:

  • Isosorbide Mononitrate

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Lactose
  • Talc
  • Silicon Dioxide
  • Cellulose, Microcrystalline
  • Aluminum Stearate

Pharmaceutical Classes:

  • Nitrate Vasodilator [EPC]
  • Nitrates [CS]
  • Vasodilation [PE]

Related Products:

Based on records with the same trade name.
  • 62175-361 Monoket 10 mg Oral Tablet by Kremers Urban Pharmaceuticals Inc.
  • 0091-3610 Monoket 10 mg Oral Tablet by Ucb, Inc.
  • 0091-3620 Monoket 20 mg Oral Tablet by Ucb, Inc.

NDC QR Code

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

NDC 62175-362 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.