NDC 59148-238 - ABILIFY MAINTENA
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 59148-238
- Package NDCs from labels
- 59148-238-90
- Manufacturer
- Otsuka America Pharmaceutical, Inc.
- Effective date
- 2026-03-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ABILIFY MAINTENA - Otsuka America Pharmaceutical, Inc. | Otsuka America Pharmaceutical, Inc. | 2026-03-24 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59148-238-90 | ABILIFY MAINTENA | 1.9 mL in 1 VIAL, SINGLE-USE | INJECTION, SUSPENSION, EXTENDED | 1.9 mL | 400 mg in 1.9mL | 27 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| aripiprazole | ACTIVE INGREDIENT | 82VFR53I78 | ABILIFY MAINTENA (ARIPIPRAZOLE) KIT [OTSUKA AMERICA PHARMACEUTICAL, INC.] | 9 | |
| aripiprazole | ACTIVE MOIETY | 82VFR53I78 | ABILIFY MAINTENA (ARIPIPRAZOLE) KIT [OTSUKA AMERICA PHARMACEUTICAL, INC.] | 9 | |
| carboxymethylcellulose sodium | INACTIVE INGREDIENT | K679OBS311 | ABILIFY MAINTENA (ARIPIPRAZOLE) KIT [OTSUKA AMERICA PHARMACEUTICAL, INC.] | 9 | |
| mannitol | INACTIVE INGREDIENT | 3OWL53L36A | ABILIFY MAINTENA (ARIPIPRAZOLE) KIT [OTSUKA AMERICA PHARMACEUTICAL, INC.] | 9 | |
| sodium hydroxide | INACTIVE INGREDIENT | 55X04QC32I | ABILIFY MAINTENA (ARIPIPRAZOLE) KIT [OTSUKA AMERICA PHARMACEUTICAL, INC.] | 9 | |
| sodium phosphate, monobasic, monohydrate | INACTIVE INGREDIENT | 593YOG76RN | ABILIFY MAINTENA (ARIPIPRAZOLE) KIT [OTSUKA AMERICA PHARMACEUTICAL, INC.] | 9 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | ABILIFY MAINTENA (ARIPIPRAZOLE) KIT [OTSUKA AMERICA PHARMACEUTICAL, INC.] | 9 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| MB CAPS | METHENAMINE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, PHENYL SALICYLATE, METHYLENE BLUE, AND HYOSCYAMINE SULFATE | Allegis Pharmaceuticals, LLC | 2efeb281-b84b-4750-e063-6394a90a27ee | 2025-02-25 | Warnings, Adverse reactions | 593YOG76RN |
| Aripiprazole | ARIPIPRAZOLE | Amneal Pharmaceuticals LLC | 7f272100-e02f-4a16-bb39-a2bf844db4f9 | 2025-02-25 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Amneal Pharmaceuticals LLC | 06dda03f-8481-46d6-af02-4f51e1a3a065 | 2025-02-20 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Unichem Pharmaceuticals (USA), Inc. | 349b8a7b-5ada-4f5c-a269-a86806c6b520 | 2025-02-20 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE ORAL | Camber Pharmaceuticals, Inc. | da47ad78-e62c-4bf3-9b53-d8cc246bcfb6 | 2025-02-19 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Alembic Pharmaceuticals Inc. | de2dc5fd-ecb4-4445-9cfb-10e64fe3269d | 2025-02-19 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Advanced Eye Relief Eye Wash | WATER SOLUTION | Bausch & Lomb Incorporated | 9caccce1-4530-441d-bf76-244edeb9dedc | 2025-02-17 | Warnings | 059QF0KO0R |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products, Inc. | 2d90c8e8-f479-3535-e063-6394a90af122 | 2025-02-07 | Warnings | 059QF0KO0R |
| Bestmade Natural Products BM63 | CEANOTHUS, KALI MUR, KALI ARS, OOPHRINUM, SELENIUM, THALLIUM, WEISBADEN | Bestmade Natural Products | 2cea4552-3700-3da3-e063-6294a90a14b5 | 2025-01-30 | Warnings | 059QF0KO0R |
| OPIPZA | ARIPIPRAZOLE | Carwin Pharmaceutical Associates, LLC | b47ede68-8942-4432-af7e-57afc14b2ba4 | 2025-01-30 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| ABILIFY | ARIPIPRAZOLE | Otsuka America Pharmaceutical, Inc. | c040bd1d-45b7-49f2-93ea-aed7220b30ac | 2025-01-29 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Lannett Company, Inc. | e7292c4c-e332-4ed4-9086-f130d223b6ae | 2025-01-24 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Direct_Rx | f823bc23-27f3-2397-e053-6294a90a365a | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Direct_Rx | f81d9b82-5879-3c0a-e053-6294a90ac23e | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Direct_Rx | facdb9a9-612f-e59a-e053-6394a90a1fa7 | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Direct_Rx | fcea91c3-e428-8991-e053-6394a90a099d | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Medics Choice Soothing Eye Wash | PURIFIED WATER | KC Pharmaceuticals, Inc. | 10e49808-161e-f4ec-e063-6294a90a1775 | 2025-01-19 | Warnings | 059QF0KO0R |
| Aripiprazole | ARIPIPRAZOLE | Bionpharma Inc. | 720bc395-777d-4e5d-9571-aad5827dbf6d | 2025-01-19 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Viona Pharmaceuticals Inc. | 73c5e380-b7b1-4362-a827-71881574ff48 | 2025-01-16 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Lubricating Tears | CARBOXYMETHYLCELLULOSE SODIUM 0.5% SOLUTION | Reliable 1 Laboritories LLC | 29023a57-eba3-4241-e063-6294a90a7048 | 2025-01-15 | Warnings | K679OBS311 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.