0173-0812 : Potiga 200 mg Oral Tablet


NDC0173-0812
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Potiga
Dosage Form: Oral Tablet, Film Coated
Application #: NDA022345
Rev. Date: 
CSA Schedule: CV (US) [1]


[1] Schedule V Controlled Substance: Low potential for abuse relative to substances listed in Schedule IV and consist primarily of preparations containing limited quantities of certain narcotics. (i.e. Cough preparations containing not more than 200 milligrams of Codeine per 100 milliliters or per 100 grams [such as Robitussin AC, Phenergan with Codeine], and Ezogabine). More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:


Markings: RTG;200
Shapes:  Oval
Colors:  Yellow
Size (mm): 14
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.

RTG 200: (0173-0812) Potiga 200 mg Oral Tablet by Glaxosmithkline LLC
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:

  • 0173-0812-59: 90 TABLET, FILM COATED IN 1 BOTTLE (0173‑0812‑59)

Active Ingredients:

  • Ezogabine

Dosage Strength:

  • 200 mg

Inactive Ingredients:

  • Croscarmellose Sodium
  • Hypromelloses
  • Ferric Oxide Yellow
  • Lecithin, Soybean
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polyvinyl Alcohol
  • Talc
  • Titanium Dioxide
  • Xanthan Gum

Pharmaceutical Classes:

  • Potassium Channel Openers [MoA]
  • Potassium Channel Opener [EPC]

Related Products:

Based on records with the same trade name.
  • 0173-0810 Potiga 50 mg Oral Tablet by Glaxosmithkline LLC
  • 0173-0813 Potiga 300 mg Oral Tablet by Glaxosmithkline LLC
  • 0173-0814 Potiga 400 mg Oral Tablet by Glaxosmithkline LLC

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