0093-3090 : Armodafinil 50 mg Oral Tablet
NDC: | 0093-3090 |
Labeler: | Teva Pharmaceuticals USA, Inc. |
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;205 |
Shapes: |
Round |
Colors: |
White |
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. |
NDC Package Codes:
- 0093-3090-56: 30 TABLET IN 1 BOTTLE (0093‑3090‑56)
Active Ingredients:
- Armodafinil
Dosage Strength:
- 50 mg
Inactive Ingredients:
- Croscarmellose Sodium
- Lactose Monohydrate
- Magnesium Stearate
- Microcrystalline Cellulose
- Povidone K30
- Starch, Corn
Related Products:
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- 59651-047 Armodafinil 200 mg Oral Tablet by Aurobindo Pharma Limited
- 61919-562 Armodafinil 150 mg Oral Tablet by Direct_rx
- 61919-770 Armodafinil 150 mg Oral Tablet by Direct_rx
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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.