Aripiprazole
- Product NDC
- 70518-2163
- 11-digit product format
- 705182163
- Labeler code
- 70518
- Product ID
- 70518-2163_c69f9ff2-a265-5883-e053-2a95a90a2687
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205064
- Marketing category
- ANDA
- Marketing start
- 2019-06-27
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2163 | ARIPIPRAZOLE TABLET [REMEDYREPACK INC.] | 5 | Legacy NDC | 20250124_c470861c-0d0f-4bc4-8c2f-c06343bcc368.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2163-0 | 70518216300 | 30 TABLET in 1 BLISTER PACK (70518-2163-0) | 30 tablet | 2019-06-27 | 0000-00-00 | No | No | Current |