47781-379 : Pregabalin Extended Release Extended Release 82.5 mg Oral Tablet, Film Coated, Extended Release


NDC: 47781-379
Labeler: Alvogen Inc.
Product Type: Human Prescription Drug
Drug Name:  Pregabalin Extended Release
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA211593
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.

NDC Package Codes:

  • 47781-379-30: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (47781‑379‑30)

Active Ingredients:

  • Pregabalin

Dosage Strength:

  • 82.5 mg

Related Products:

Based on records with the same trade name.
  • 47781-380 Pregabalin Extended Release Extended Release 165 mg Oral Tablet, Film Coated, Extended Release by Alvogen Inc.
  • 47781-381 Pregabalin Extended Release Extended Release 330 mg Oral Tablet, Film Coated, Extended Release by Alvogen Inc.
  • 50228-462 Pregabalin Extended Release Extended Release 82.5 mg Oral Tablet, Film Coated, Extended Release by Sciegen Pharmaceuticals, Inc.
  • 50228-463 Pregabalin Extended Release Extended Release 165 mg Oral Tablet, Film Coated, Extended Release by Sciegen Pharmaceuticals, Inc.
  • 50228-464 Pregabalin Extended Release Extended Release 330 mg Oral Tablet, Film Coated, Extended Release by Sciegen Pharmaceuticals, Inc.

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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.