ARIPIPRAZOLE
- Product NDC
- 70518-2515
- 11-digit product format
- 705182515
- Labeler code
- 70518
- Product ID
- 70518-2515_c9c51a5b-cd1e-00a5-e053-2995a90a6f63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205363
- Marketing category
- ANDA
- Marketing start
- 2019-12-31
- 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 |
|---|
| 70518-2515-0 | 70518251500 | 30 POUCH in 1 BOX (70518-2515-0) > 1 TABLET in 1 POUCH (70518-2515-1) | 30 pouch | 2019-12-31 | 0000-00-00 | No | No | Current |