Aripiprazole
- Product NDC
- 63739-413
- 11-digit product format
- 637390413
- Labeler code
- 63739
- Product ID
- 63739-413_b466e9af-1a1d-5026-e053-2995a90a92a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA203908
- Marketing category
- ANDA
- Marketing start
- 2015-10-08
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63739-413-10 | 63739041310 | 100 TABLET in 1 BOTTLE (63739-413-10) | 100 tablet | 2019-01-21 | 0000-00-00 | No | No | Current |