Aripiprazole
- Product NDC
- 68071-2676
- 11-digit product format
- 680712676
- Labeler code
- 68071
- Product ID
- 68071-2676_dd45a23a-08ea-055b-e053-2a95a90a14ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA207105
- Marketing category
- ANDA
- Marketing start
- 2019-02-27
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2676-4 | Aripiprazole | 14 in 1 BOTTLE | TABLET | 14 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2676 | ARIPIPRAZOLE TABLET [NUCARE PHARMACEUTICALS,INC.] | 2 | Legacy NDC, 1 package rows | 20230715_dd45a23a-08eb-055b-e053-2a95a90a14ac.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 |
|---|
| 68071-2676-4 | 68071267604 | 14 TABLET in 1 BOTTLE (68071-2676-4) | 14 tablet | 2022-04-22 | 0000-00-00 | No | No | Current |