ARMODAFINIL
- Product NDC
- 72189-353
- 11-digit product format
- 721890353
- Labeler code
- 72189
- Product ID
- 72189-353_2c4c8cee-041f-c5ef-e063-6394a90a8cfd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ARMODAFINIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRx
- Application
- NDA021875
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2022-04-29
- Substance
- ARMODAFINIL
- Active strength
- 200 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ARMODAFINIL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARMODAFINIL | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V63XWA605I |
| Rxcui | 861960 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-353-30 | ARMODAFINIL | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-353 | ARMODAFINIL TABLET [DIRECTRX] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250123_ddd06dab-0855-5b4e-e053-2a95a90a5e67.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 |
|---|
| 72189-353-30 | 72189035330 | 30 TABLET in 1 BOTTLE (72189-353-30) | 30 tablet | 2022-04-29 | 0000-00-00 | No | No | Current |