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 |
|---|---|---|---|---|---|---|
| aripiprazole | ARIPIPRAZOLE | Proficient Rx LP | a3c0be94-c6c0-47e2-892f-c51f100fb3a3 | 2025-08-01 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Focus Tears PF | CARBOXYMETHYLCELLULOSE SODIUM | Covalent Medical | 772c7070-82ff-4371-b071-940ff91372c6 | 2025-07-17 | Warnings | K679OBS311 |
| Sterile Water | STERILE WATER | Nephron Pharmaceuticals Corporation | bc04a883-babc-87a6-e053-2995a90a3dfd | 2025-07-11 | Warnings, Adverse reactions | 059QF0KO0R |
| InterSol | PLATELET ADDITIVE 3 | Fenwal, Inc. | 17dec820-1b57-4ac9-82a8-419cab664a2f | 2025-06-27 | Warnings, Adverse reactions | 593YOG76RN |
| Aripiprazole | ARIPIPRAZOLE | Alembic Pharmaceuticals Inc. | a10a5427-58b1-42dd-964c-3f8c78770534 | 2025-06-25 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Plaque identifying | PLAQUE IDENTIFYING | Shenzhen Yagao Technology Co., Ltd. | 37eeb656-22f1-7372-e063-6394a90ad041 | 2025-06-19 | Warnings | 059QF0KO0R |
| Aripiprazole | ARIPIPRAZOLE | NuCare Pharmaceuticals,Inc. | 3726d102-dd9f-645e-e063-6294a90aeb9e | 2025-06-09 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | A-S Medication Solutions | a8edb057-18a3-446d-8af0-672c97933a88 | 2025-06-03 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Sterile Water | WATER | Henry Schein, Inc. | 88403fcf-a276-42c0-88b6-bd84a720b564 | 2025-05-29 | Warnings, Adverse reactions | 059QF0KO0R |
| aripiprazole | ARIPIPRAZOLE | ST. MARY'S MEDICAL PARK PHARMACY | 35a86989-862e-b0bb-e063-6394a90a7ec1 | 2025-05-21 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Mannitol | MANNITOL | Henry Schein, Inc. | e2444db1-9dfe-451f-a33c-9b00786464d2 | 2025-05-20 | Warnings, Adverse reactions | 3OWL53L36A |
| Aripiprazole | ARIPIPRAZOLE | Chartwell RX, LLC | 1d27462e-45c7-4335-9092-84c340e06a2c | 2025-05-16 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Eyesaline Emergency Eyewash | STERILE EYESALINE EYEWASH | Honeywell Safety Products USA, Inc. | 2d567518-4c54-7448-e063-6294a90a3e64 | 2025-05-14 | Warnings | 059QF0KO0R |
| Aripiprazole | ARIPIPRAZOLE | Bryant Ranch Prepack | 385301f5-e59d-42d5-8544-aadf0ee0c967 | 2025-04-29 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Abilify Asimtufii | ARIPIPRAZOLE | Otsuka America Pharmaceutical, Inc | da4c07fd-1130-4341-bb44-63acfa4162be | 2025-04-04 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Eye Wash | WATER | CMC Group Inc. | 6158a1f5-a6bc-4a3e-9d1d-0a310d9dc561 | 2025-04-02 | Warnings | 059QF0KO0R |
| aripiprazole | ARIPIPRAZOLE | Torrent Pharmaceuticals Limited | 3988e66f-339c-451e-9f8a-9d0c0a2a381b | 2025-03-28 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Macleods Pharmaceuticals Limited | ab4245a1-71f7-45be-a2ef-b0636ed3cc20 | 2025-03-24 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Bestmade Natural Products Field of Flowers Formula | AESCULUS CAR, AESCULUS HIP, AGRIMONIA EUP, BROMUS RAM, CALLUNA VULG, CARPINUS BET, CASTANEA SAT, CENTAURIUM UMB, CERATOSTIGMA WILLM, CICHORIUM INT, CLEMATIS VIT, FAGUS SYLV, GENTIANELLA AMARELLA, HELIANTHEMUM NUMMULARIUM, ILEX AQUIFOLIUM, IMPATIENS GLAND, LARIX DECIDUA, LONICERA CAPRIFOLIUM, MALUS, MIMULUS GUT, OLEA EUROP, ORNITHOGALUM UMB, PINUS SYL, POPULUS TREM, PRUNUS CERA, QUERCUS ROB, ROCK WATER, ROSA CAN, SALIX VIT, SCLERANTHUS ANNNUS, SINAPIS ARV, ULEX EURO, ULMUS PROC, VERBENA, VITIS VIN | Bestmade Natural Products | 2fbf9b7c-e54f-589d-e063-6394a90a14a7 | 2025-03-07 | Warnings | 059QF0KO0R |
| AeroWash Eyewash | EYEWASH SOLUTION | Aero Healthcare US LLC | a477de08-4301-0ee5-e053-2995a90af79d | 2025-02-26 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.