Aripiprazole
- Product NDC
- 70518-2565
- 11-digit product format
- 705182565
- Labeler code
- 70518
- Product ID
- 70518-2565_ca625670-6522-92e7-e053-2995a90a5048
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204838
- Marketing category
- ANDA
- Marketing start
- 2020-02-04
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 30 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 |
|---|
| 70518-2565-0 | 70518256500 | 30 POUCH in 1 BOX (70518-2565-0) > 1 TABLET in 1 POUCH (70518-2565-1) | 30 pouch | 2020-02-04 | 0000-00-00 | No | No | Current |