NDC 71335-1173 – Modafinil
Modafinil 200 mg/1 · Tablet · Oral
Product NDC71335-1173
Product details
- Brand name
- Modafinil
- Generic name
- Modafinil
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202566
- Marketed since
- September 27, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sympathomimetic-like Agent
Active ingredients
- Modafinil 200 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1173-0 | 100 TABLET in 1 BOTTLE (71335-1173-0) | Jul 9, 2024 |
| 71335-1173-1 | 30 TABLET in 1 BOTTLE (71335-1173-1) | Apr 2, 2019 |
| 71335-1173-2 | 18 TABLET in 1 BOTTLE (71335-1173-2) | Jul 9, 2024 |
| 71335-1173-3 | 16 TABLET in 1 BOTTLE (71335-1173-3) | Jul 9, 2024 |
| 71335-1173-4 | 8 TABLET in 1 BOTTLE (71335-1173-4) | Jul 9, 2024 |
| 71335-1173-5 | 10 TABLET in 1 BOTTLE (71335-1173-5) | Jul 9, 2024 |
| 71335-1173-6 | 60 TABLET in 1 BOTTLE (71335-1173-6) | Jun 5, 2019 |
| 71335-1173-7 | 90 TABLET in 1 BOTTLE (71335-1173-7) | Jul 9, 2024 |
| 71335-1173-8 | 45 TABLET in 1 BOTTLE (71335-1173-8) | Jul 9, 2024 |
| 71335-1173-9 | 180 TABLET in 1 BOTTLE (71335-1173-9) | Jul 9, 2024 |
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