NDC 71335-2501 – Modafinil
Modafinil 200 mg/1 · Tablet · Oral
Product NDC71335-2501
Product details
- Brand name
- Modafinil
- Generic name
- Modafinil
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207196
- Marketed since
- February 21, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sympathomimetic-like Agent
Active ingredients
- Modafinil 200 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2501-0 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2501-0) | Sep 23, 2024 |
| 71335-2501-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2501-1) | Sep 23, 2024 |
| 71335-2501-2 | 18 TABLET in 1 BOTTLE, PLASTIC (71335-2501-2) | Sep 23, 2024 |
| 71335-2501-3 | 16 TABLET in 1 BOTTLE, PLASTIC (71335-2501-3) | Sep 23, 2024 |
| 71335-2501-4 | 8 TABLET in 1 BOTTLE, PLASTIC (71335-2501-4) | Sep 23, 2024 |
| 71335-2501-5 | 10 TABLET in 1 BOTTLE, PLASTIC (71335-2501-5) | Sep 23, 2024 |
| 71335-2501-6 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2501-6) | Sep 23, 2024 |
| 71335-2501-7 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2501-7) | Sep 23, 2024 |
| 71335-2501-8 | 45 TABLET in 1 BOTTLE, PLASTIC (71335-2501-8) | Sep 23, 2024 |
| 71335-2501-9 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-2501-9) | Sep 23, 2024 |
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