aripiprazole
- Product NDC
- 68071-5062
- 11-digit product format
- 680715062
- Labeler code
- 68071
- Product ID
- 68071-5062_bbb678c8-7781-93ad-e053-2a95a90af9d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2015-04-28
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5062-9 | 68071506209 | 90 TABLET in 1 BOTTLE (68071-5062-9) | 90 tablet | 2019-09-16 | 0000-00-00 | No | No | Current |