ARIPIPRAZOLE
- Product NDC
- 31722-919
- 11-digit product format
- 317220919
- Labeler code
- 31722
- Product ID
- 31722-919_c99f3445-aceb-47c7-9f35-4f906aad08aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- ANDA205064
- Marketing category
- ANDA
- Marketing start
- 2017-08-08
- Substance
- ARIPIPRAZOLE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ARIPIPRAZOLE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARIPIPRAZOLE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 82VFR53I78 |
| Rxcui | 349490, 349545, 349547, 349553, 402131, 602964 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 31722-919-01 | ARIPIPRAZOLE | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 31722-919-30 | ARIPIPRAZOLE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-919 | ARIPIPRAZOLE TABLET [CAMBER PHARMACEUTICALS, INC.] | 1 | Current NDC, 2 package rows | 20230321_3718e585-06b9-40fd-a3eb-18b6497a4235.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 31722-919-01 | 31722091901 | 100 TABLET in 1 BOTTLE (31722-919-01) | 100 tablet | 2017-08-08 | No | No | Current |
| 31722-919-30 | 31722091930 | 30 TABLET in 1 BOTTLE (31722-919-30) | 30 tablet | 2017-08-08 | No | No | Current |