Aripiprazole
- Product NDC
- 63739-074
- 11-digit product format
- 637390074
- Labeler code
- 63739
- Product ID
- 63739-074_f1d7e020-1723-6a0e-e053-2a95a90a0de2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA205064
- Marketing category
- ANDA
- Marketing start
- 2021-11-09
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-074 | ARIPIPRAZOLE TABLET [MCKESSON CORPORATION DBA SKY PACKAGING] | 5 | Legacy NDC | 20241222_d05fcc78-c7bc-386e-e053-2995a90a6dbd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-074-10 | 63739007410 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-074-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2021-11-09 | 0000-00-00 | No | No | Current |