NDC 23155-862 – Modafinil
Modafinil 200 mg/1 · Tablet · Oral
Product NDC23155-862
Product details
- Brand name
- Modafinil
- Generic name
- Modafinil
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207196
- Marketed since
- February 21, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Sympathomimetic-like Agent
Active ingredients
- Modafinil 200 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 23155-862-01 | 100 TABLET in 1 BOTTLE (23155-862-01) | Feb 21, 2024 |
| 23155-862-03 | 30 TABLET in 1 BOTTLE (23155-862-03) | Feb 21, 2024 |
| 23155-862-05 | 500 TABLET in 1 BOTTLE (23155-862-05) | Feb 21, 2024 |
| 23155-862-09 | 90 TABLET in 1 BOTTLE (23155-862-09) | Feb 21, 2024 |
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