Aripiprazole
- Product NDC
- 16714-142
- 11-digit product format
- 167140142
- Labeler code
- 16714
- Product ID
- 16714-142_04230bfc-e6ad-1844-e063-6394a90a939e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA205064
- Marketing category
- ANDA
- Marketing start
- 2020-10-01
- Substance
- ARIPIPRAZOLE
- Active strength
- 5 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 | 5 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 |
|---|
| 16714-142-01 | 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 |
|---|
| 16714-142 | ARIPIPRAZOLE (ARIPIPRAZOLE) TABLET [NORTHSTAR RXLLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230831_f87dbfe4-5417-47c9-a97f-d246cfc10023.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 |
|---|
| 16714-142-01 | 16714014201 | 30 TABLET in 1 BOTTLE (16714-142-01) | 30 tablet | 2020-10-01 | 0000-00-00 | No | No | Current |