Rexulti
- Product NDC
- 75929-273
- 11-digit product format
- 759290273
- Labeler code
- 75929
- Product ID
- 75929-273_4b1b593e-c89a-821e-e063-6394a90a06cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- brexpiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pharma Packaging Solutions, LLC dba Tjoapack LLC
- Application
- NDA205422
- Marketing category
- NDA
- Marketing start
- 2015-07-10
- Substance
- BREXPIPRAZOLE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rexulti
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BREXPIPRAZOLE | 2 mg/1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 75929-273-03 | 75929027303 | 1 BOTTLE in 1 CARTON (75929-273-03) / 30 TABLET in 1 BOTTLE | 1 bottle | 2015-07-10 | No | No | Current |