Aripiprazole
- Product NDC
- 72189-455
- 11-digit product format
- 721890455
- Labeler code
- 72189
- Product ID
- 72189-455_2c4dbbad-3ed7-fec3-e063-6394a90a3b4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2023-03-30
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 82VFR53I78 |
| Rxcui | 349553 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-455-30 | Aripiprazole | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-455 | ARIPIPRAZOLE TABLET [DIRECT_RX] | 2 | Current NDC, 1 package rows | 20250123_f81d9b82-5879-3c0a-e053-6294a90ac23e.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 |
|---|
| 72189-455-30 | 72189045530 | 30 TABLET in 1 BOTTLE (72189-455-30) | 30 tablet | 2023-03-30 | No | No | Historical |