Aripiprazole
- Product NDC
- 0615-8259
- 11-digit product format
- 006158259
- Labeler code
- 0615
- Product ID
- 0615-8259_ac749cd0-19ac-4dbc-9c2b-26d3d164e8b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA206383
- Marketing category
- ANDA
- Marketing start
- 2016-09-29
- Marketing end
- 2022-08-31
- Substance
- ARIPIPRAZOLE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8259-39 | 00615825939 | 30 TABLET in 1 BLISTER PACK (0615-8259-39) | 30 tablet | 2019-01-14 | 2022-08-31 | No | No | Current |