0173-0810 : Potiga 50 mg Oral Tablet


NDC: 0173-0810
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;50
Shapes:  Round
Colors:  Purple
Size (mm): 6
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 50: (0173-0810) Potiga 50 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:

  • 0173-0810-59: 90 TABLET, FILM COATED IN 1 BOTTLE (0173‑0810‑59)
  • 0173-0810-62: 2 BOTTLE IN 1 CARTON (0173‑0810‑62) > 90 TABLET, FILM COATED IN 1 BOTTLE (0173‑0810‑01)
  • 0173-0810-63: 105 TABLET, FILM COATED IN 1 BLISTER PACK (0173‑0810‑63)

Active Ingredients:

  • Ezogabine

Dosage Strength:

  • 50 mg

Inactive Ingredients:

  • Cochineal
  • Croscarmellose Sodium
  • Fd&c Blue No. 2
  • Hypromelloses
  • 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.
  • 0173-0812 Potiga 200 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

NDC QR Code

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NDC 0173-0810 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.