ARMODAFINIL
- Product NDC
- 61919-562
- 11-digit product format
- 619190562
- Labeler code
- 61919
- Product ID
- 61919-562_85a29824-058c-1411-e053-2a91aa0a451b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ARMODAFINIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- NDA021875
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-04-03
- Marketing end
- 0000-00-00
- Substance
- ARMODAFINIL
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-562-30 | ARMODAFINIL | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-562 | ARMODAFINIL TABLET ARMODAFINIL TABLET [DIRECT_RX] | 2 | Legacy NDC, 1 package rows | 20190404_7ea5430a-df28-e521-e053-2a91aa0a8f22.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-562-30 | 61919056230 | 30 in 1 BOTTLE | Historical |