ARMODAFINIL
- Product NDC
- 72189-041
- 11-digit product format
- 721890041
- Labeler code
- 72189
- Product ID
- 72189-041_91e82344-ef84-a838-e053-2995a90abd38
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ARMODAFINIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA206069
- Marketing category
- ANDA
- Marketing start
- 2019-09-06
- Marketing end
- 0000-00-00
- Substance
- ARMODAFINIL
- Active strength
- 150 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-041-30 | ARMODAFINIL | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-041 | ARMODAFINIL TABLET [DIRECT_RX] | 1 | Legacy NDC, 1 package rows | 20191101_91e82344-ef83-a838-e053-2995a90abd38.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 |
|---|
| 72189-041-30 | 72189004130 | 30 TABLET in 1 BOTTLE (72189-041-30) | 30 tablet | 2019-09-06 | 0000-00-00 | No | No | Current |