Aripiprazole
- Product NDC
- 70518-2150
- 11-digit product format
- 705182150
- Labeler code
- 70518
- Product ID
- 70518-2150_49d9bcfb-fe1e-d5b5-e063-6294a90ac4ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202101
- Marketing category
- ANDA
- Marketing start
- 2019-06-24
- Substance
- ARIPIPRAZOLE
- Active strength
- 5 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 | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 82VFR53I78 |
| Rxcui | 402131 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2150-0 | Aripiprazole | 100 in 1 BOX | TABLET | 100 | | 5 |
| 70518-2150-1 | Aripiprazole | 1 in 1 POUCH | TABLET | 1 | | 5 |
| 70518-2150-2 | Aripiprazole | 30 in 1 BLISTER PACK | TABLET | 30 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-2150-0 | 70518215000 | 100 in 1 BOX | | | | | Historical |
| 70518-2150-1 | 70518215001 | 1 in 1 POUCH | | | | | Historical |
| 70518-2150-2 | 70518215002 | 30 TABLET in 1 BLISTER PACK (70518-2150-2) | 30 tablet | 2025-07-08 | No | No | Historical |