Aripiprazole
- Product NDC
- 71335-1515
- 11-digit product format
- 713351515
- Labeler code
- 71335
- Product ID
- 71335-1515_3b42a741-e614-4c5d-a928-6451e12235ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206174
- Marketing category
- ANDA
- Marketing start
- 2017-05-30
- Substance
- ARIPIPRAZOLE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aripiprazole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARIPIPRAZOLE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 82VFR53I78 |
| Rxcui | 349545 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1515 | ARIPIPRAZOLE TABLET [BRYANT RANCH PREPACK] | 102 | Current NDC, Legacy NDC, 4 package rows | 20240410_69af5199-f872-4298-8d09-035e2127d3d4.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 |
|---|
| 71335-1515-1 | 71335151501 | 30 TABLET in 1 BOTTLE (71335-1515-1) | 30 tablet | 2020-03-16 | 0000-00-00 | No | No | Current |
| 71335-1515-2 | 71335151502 | 60 TABLET in 1 BOTTLE (71335-1515-2) | 60 tablet | 2024-04-03 | 0000-00-00 | No | No | Current |
| 71335-1515-3 | 71335151503 | 28 TABLET in 1 BOTTLE (71335-1515-3) | 28 tablet | 2024-04-03 | 0000-00-00 | No | No | Current |
| 71335-1515-4 | 71335151504 | 90 TABLET in 1 BOTTLE (71335-1515-4) | 90 tablet | 2024-04-03 | 0000-00-00 | No | No | Current |