Aripiprazole
- Product NDC
- 17856-0110
- 11-digit product format
- 178560110
- Labeler code
- 17856
- Product ID
- 17856-0110_c046249a-b2cb-4e67-ade6-c517766c4606
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA210479
- Marketing category
- ANDA
- Marketing start
- 2019-04-12
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0110-1 | Aripiprazole | 72 in 1 BOX, UNIT-DOSE | SOLUTION | 72 | | 2 |
| 17856-0110-1 | Aripiprazole | 5 mL in 1 CUP, UNIT-DOSE | SOLUTION | 5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0110 | ARIPIPRAZOLE SOLUTION [ATLANTIC BIOLOGICALS CORP.] | 2 | Legacy NDC, 2 package rows | 20210112_48d8b880-ed1c-425a-88ef-75289d51e126.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-0110-1 | 17856011001 | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0110-1) > 5 mL in 1 CUP, UNIT-DOSE | 2021-01-11 | 0000-00-00 | No | No | Current |