Aripiprazole
- Product NDC
- 0904-7370
- 11-digit product format
- 009047370
- Labeler code
- 0904
- Product ID
- 0904-7370_face01d9-5df3-4581-a4e7-e692444768a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA204838
- Marketing category
- ANDA
- Marketing start
- 2016-06-20
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aripiprazole
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARIPIPRAZOLE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 82VFR53I78 |
| Rxcui | 349490, 349545, 349547, 349553, 402131, 602964 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-7370-04 | Aripiprazole | 30 in 1 CARTON | TABLET | 30 | | 4 |
| 0904-7370-04 | Aripiprazole | 1 in 1 BLISTER PACK | TABLET | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7370 | ARIPIPRAZOLE TABLET [MAJOR PHARMACEUTICALS] | 3 | Current NDC, 2 package rows | 20250330_573c6bb6-941f-4413-8c23-826025385864.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0904-7370-04 | 00904737004 | 30 BLISTER PACK in 1 CARTON (0904-7370-04) / 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2023-10-01 | No | No | Current |