Aripiprazole
- Product NDC
- 42043-401
- 11-digit product format
- 420430401
- Labeler code
- 42043
- Product ID
- 42043-401_41e54894-5e27-4acb-8bb3-e61c9e5ddfdd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- OrchidPharma Inc
- Application
- ANDA202547
- Marketing category
- ANDA
- Marketing start
- 2018-11-15
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 15 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42043-401-03 | 42043040103 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (42043-401-03) | 2018-11-15 | 0000-00-00 | No | No | Current |