59651-047 : Armodafinil 200 mg Oral Tablet


NDC: 59651-047
Labeler: Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Drug Name:  Armodafinil
Dosage Form: Oral Tablet
Application #: NDA021875
Rev. Date: 
CSA Schedule: CIV (US) [1]


[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:


Markings: C;220
Shapes:  Rectangle (4 sides)
Colors:  White
Size (mm): 12
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.

NDC Package Codes:

  • 59651-047-30: 30 TABLET IN 1 BOTTLE (59651‑047‑30)

Active Ingredients:

  • Armodafinil

Dosage Strength:

  • 200 mg

Inactive Ingredients:

  • Croscarmellose Sodium
  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Povidone K29/32
  • Starch, Corn

Related Products:

Based on records with the same trade name.
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  • 65862-807 Armodafinil 250 mg Oral Tablet by Aurobindo Pharma Limited
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  • 0781-8053 Armodafinil 250 mg Oral Tablet by Sandoz Inc.
  • 51991-322 Armodafinil 50 mg Oral Tablet by Breckenridge Pharmaceutical, Inc.
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NDC 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.