aripiprazole
- Product NDC
- 63629-7003
- 11-digit product format
- 636297003
- Labeler code
- 63629
- Product ID
- 63629-7003_19629960-f7d5-434b-869d-6784b2a65c74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2015-04-28
- 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 |
|---|
| 63629-7003 | ARIPIPRAZOLE TABLET [BRYANT RANCH PREPACK] | 105 | Current NDC, Legacy NDC, 4 package rows | 20241109_b62837db-1949-4dba-9e2f-714a9f136f5a.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 |
|---|
| 63629-7003-1 | 63629700301 | 30 TABLET in 1 BOTTLE (63629-7003-1) | 30 tablet | 2016-05-16 | 0000-00-00 | No | No | Current |
| 63629-7003-2 | 63629700302 | 60 TABLET in 1 BOTTLE (63629-7003-2) | 60 tablet | 2024-10-29 | 0000-00-00 | No | No | Current |
| 63629-7003-3 | 63629700303 | 28 TABLET in 1 BOTTLE (63629-7003-3) | 28 tablet | 2024-10-29 | 0000-00-00 | No | No | Current |
| 63629-7003-4 | 63629700304 | 90 TABLET in 1 BOTTLE (63629-7003-4) | 90 tablet | 2017-12-26 | 0000-00-00 | No | No | Current |