Aripiprazole
- Product NDC
- 70518-3090
- 11-digit product format
- 705183090
- Labeler code
- 70518
- Product ID
- 70518-3090_4e9166bd-b9e4-2c8a-e063-6294a90aea1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207105
- Marketing category
- ANDA
- Marketing start
- 2021-05-10
- Substance
- ARIPIPRAZOLE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aripiprazole
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARIPIPRAZOLE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 82VFR53I78 |
| Rxcui | 602964 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3090-0 | Aripiprazole | 30 in 1 BLISTER PACK | TABLET | 30 | | 9 |
| 70518-3090-1 | Aripiprazole | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3090 | ARIPIPRAZOLE TABLET [REMEDYREPACK INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250523_6f580e75-61ab-4c7b-bb3f-f027a9603f84.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 |
|---|
| 70518-3090-0 | 70518309000 | 30 TABLET in 1 BLISTER PACK (70518-3090-0) | 30 tablet | 2021-05-10 | 0000-00-00 | No | No | Current |
| 70518-3090-1 | 70518309001 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-3090-1) | 30 tablet | 2025-07-01 | | No | No | Historical |