NDC 87063-309 – Modafinil
Modafinil 200 mg/1 · Tablet · Oral
Product NDC87063-309
Product details
- Brand name
- Modafinil
- Generic name
- Modafinil
- Labeler
- ASCLEMED USA INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209966
- Marketed since
- February 15, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Sympathomimetic-like Agent
Active ingredients
- Modafinil 200 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 87063-309-01 | 100 TABLET in 1 BOTTLE (87063-309-01) | Sep 10, 2026 |
| 87063-309-30 | 30 TABLET in 1 BOTTLE (87063-309-30) | Sep 10, 2026 |
| 87063-309-60 | 60 TABLET in 1 BOTTLE (87063-309-60) | Sep 10, 2026 |
| 87063-309-90 | 90 TABLET in 1 BOTTLE (87063-309-90) | Sep 10, 2026 |
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