Armodafinil
- Product NDC
- 71335-2991
- 11-digit product format
- 713352991
- Labeler code
- 71335
- Product ID
- 71335-2991_7e8152cc-4061-4276-8843-a06cbfb5b1bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- armodafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200043
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- Substance
- ARMODAFINIL
- Active strength
- 150 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Armodafinil
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARMODAFINIL | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V63XWA605I |
| Rxcui | 724859 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2991-1 | Armodafinil | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 71335-2991-2 | Armodafinil | 28 in 1 BOTTLE | TABLET | 28 | | 1 |
| 71335-2991-3 | Armodafinil | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2991-1 | 71335299101 | 30 TABLET in 1 BOTTLE (71335-2991-1) | 30 tablet | 2026-02-04 | No | No | Historical |
| 71335-2991-2 | 71335299102 | 28 TABLET in 1 BOTTLE (71335-2991-2) | 28 tablet | 2026-02-04 | No | No | Historical |
| 71335-2991-3 | 71335299103 | 90 TABLET in 1 BOTTLE (71335-2991-3) | 90 tablet | 2026-02-04 | No | No | Historical |