Aripiprazole
- Product NDC
- 0904-6513
- 11-digit product format
- 009046513
- Labeler code
- 0904
- Product ID
- 0904-6513_b57698aa-42fb-43eb-84bc-8c20a358a946
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078583
- Marketing category
- ANDA
- Marketing start
- 2015-08-25
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-6513 | ARIPIPRAZOLE TABLET [MAJOR PHARMACEUTICALS] | 7 | Legacy NDC | 20240920_3279b9dc-8efd-463b-8f15-e26162ed78e3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6513-04 | 00904651304 | 30 BLISTER PACK in 1 CARTON (0904-6513-04) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2015-08-25 | 0000-00-00 | No | No | Current |