Armodafinil
- Product NDC
- 0781-8029
- 11-digit product format
- 007818029
- Labeler code
- 0781
- Product ID
- 0781-8029_dea0ad34-a35f-42ba-a6b6-dea58a16868f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Armodafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- NDA021875
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-12-01
- Marketing end
- 2027-09-30
- Substance
- ARMODAFINIL
- Active strength
- 50 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Armodafinil
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARMODAFINIL | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V63XWA605I |
| Rxcui | 724859, 724861, 724863, 861960 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0781-8029-31 | Armodafinil | 30 in 1 BOTTLE | TABLET | 30 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-8029 | ARMODAFINIL TABLET [SANDOZ INC] | 14 | Current NDC, Legacy NDC, 1 package rows | 20240828_a3341ec8-1ad4-49e2-922b-13d1b30c8c1d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-8029-31 | 00781802931 | 30 TABLET in 1 BOTTLE (0781-8029-31) | 30 tablet | 2016-12-01 | 2027-09-30 | No | No | Current |