NDC 70771-1052 – Modafinil
Modafinil 200 mg/1 · Tablet · Oral
Product NDC70771-1052
Product details
- Brand name
- Modafinil
- Generic name
- Modafinil
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209966
- Marketed since
- January 4, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sympathomimetic-like Agent
Active ingredients
- Modafinil 200 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1052-1 | 100 TABLET in 1 BOTTLE (70771-1052-1) | Jan 4, 2018 |
| 70771-1052-3 | 30 TABLET in 1 BOTTLE (70771-1052-3) | Jan 4, 2018 |
| 70771-1052-9 | 90 TABLET in 1 BOTTLE (70771-1052-9) | Jan 4, 2018 |
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