50090-1250 : Tekturna 300 mg Oral Tablet, Film Coated


NDC: 50090-1250
Labeler: A-s Medication Solutions
Product Type: Human Prescription Drug
Drug Name:  Tekturna
Dosage Form: Oral Tablet, Film Coated
Application #: NDA021985
Rev. Date: 


Appearance:


Markings: NVR;IU
Shapes:  Oval
Colors:  Red
Size (mm): 18
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NVR IU: (0078-0486) Tekturna 300 mg Oral Tablet, Film Coated by A-s Medication Solutions
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:

  • 50090-1250-0: 30 TABLET, FILM COATED IN 1 BOTTLE (50090‑1250‑0)

Active Ingredients:

  • Aliskiren Hemifumarate

Dosage Strength:

  • 300 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Crospovidone (15 Mpa.s At 5%)
  • Hypromellose, Unspecified
  • Ferric Oxide Red
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Polyethylene Glycol, Unspecified
  • Talc
  • Titanium Dioxide
  • Ferrosoferric Oxide

Pharmaceutical Classes:

  • Renin Inhibitor [EPC]
  • Renin Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 50090-2985 Tekturna 300 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 54569-6274 Tekturna 300 mg Oral Tablet, Film Coated by A-s Medication Solutions
  • 0078-0485 Tekturna 150 mg Oral Tablet by Novartis Pharmaceuticals Corporation
  • 0078-0486 Tekturna 300 mg Oral Tablet by Novartis Pharmaceuticals Corporation
  • 54868-5772 Tekturna 150 mg Oral Tablet by Physicians Total Care, Inc.
  • 54868-6042 Tekturna 300 mg Oral Tablet by Physicians Total Care, Inc.
  • 69189-0485 Tekturna 150 mg Oral Tablet, Film Coated by Avera Mckennan Hospital
  • 70839-150 Tekturna 150 mg Oral Tablet, Film Coated by Noden Pharma USA, Inc.
  • 70839-300 Tekturna 300 mg Oral Tablet, Film Coated by Noden Pharma USA, Inc.

NDC QR Code

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NDC 50090-1250 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.