NDC 0781-8037 – Armodafinil
Armodafinil 150 mg/1 · Tablet · Oral
Product NDC0781-8037
Product details
- Brand name
- Armodafinil
- Generic name
- Armodafinil
- Labeler
- Sandoz Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA021875
- Marketed since
- December 1, 2016
- Marketing end
- June 30, 2028
Active ingredients
- Armodafinil 150 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0781-8037-31 | 30 TABLET in 1 BOTTLE (0781-8037-31) | Dec 1, 2016 |
Other Armodafinil products
- 65862-998 Armodafinil 200 mg/1 · Tablet · Aurobindo Pharma Limited
- 65862-805 Armodafinil 50 mg/1 · Tablet · Aurobindo Pharma Limited
- 65862-806 Armodafinil 150 mg/1 · Tablet · Aurobindo Pharma Limited
- 65862-807 Armodafinil 250 mg/1 · Tablet · Aurobindo Pharma Limited
- 71335-1308 Armodafinil 250 mg/1 · Tablet · Bryant Ranch Prepack
- 71335-1193 Armodafinil 150 mg/1 · Tablet · Bryant Ranch Prepack
- 71335-2991 Armodafinil 150 mg/1 · Tablet · Bryant Ranch Prepack
- 72189-133 Armodafinil 250 mg/1 · Tablet · direct rx
- 72189-261 Armodafinil 250 mg/1 · Tablet · direct rx
- 72189-464 Armodafinil 50 mg/1 · Tablet · Direct_Rx
- 72189-353 Armodafinil 200 mg/1 · Tablet · DirectRx
- 0378-3432 Armodafinil 150 mg/1 · Tablet · Mylan Pharmaceuticals Inc.