68788-7593 : Armodafinil 250 mg Oral Tablet


NDC: 68788-7593
Labeler: Preferred Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Armodafinil
Dosage Form: Oral Tablet
Application #: ANDA206069
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: K;60
Shapes:  Oval
Colors:  White
Size (mm): 16
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:

  • 68788-7593-3: 30 TABLET IN 1 BOTTLE (68788‑7593‑3)
  • 68788-7593-6: 60 TABLET IN 1 BOTTLE (68788‑7593‑6)
  • 68788-7593-9: 90 TABLET IN 1 BOTTLE (68788‑7593‑9)

Active Ingredients:

  • Armodafinil

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Croscarmellose Sodium
  • Lactose Monohydrate
  • Magnesium Stearate
  • Povidone K30 /

Related Products:

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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.