Aripiprazole
- Product NDC
- 48433-117
- 11-digit product format
- 484330117
- Labeler code
- 48433
- Product ID
- 48433-117_3faad38f-c24b-4bcc-a602-a6d1dc99bfbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Safecor Health, LLC
- Application
- ANDA078583
- Marketing category
- ANDA
- Marketing start
- 2015-12-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48433-117-10 | 48433011710 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (48433-117-10) > 10 TABLET in 1 BLISTER PACK (48433-117-01) | 10 blister pack | 2015-12-01 | 0000-00-00 | No | No | Current |