NDC 59148-235 - 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
- 59148-235
- Package NDCs from labels
- 59148-235-70
- 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 |
|---|---|---|---|---|---|---|
| 59148-235-70 | ABILIFY MAINTENA | 1.5 mL in 1 VIAL, SINGLE-USE | INJECTION, SUSPENSION, EXTENDED | 1.5 mL | 300 mg in 1.5mL | 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#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Aripiprazole | ARIPIPRAZOLE | REMEDYREPACK INC. | bc3fde41-2f24-44e2-815d-15fe55bd68b3 | 2026-07-30 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | REMEDYREPACK INC. | 506fa28f-6f98-4632-bce8-72a9cb507c90 | 2026-07-29 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | REMEDYREPACK INC. | f713c38e-cc49-4243-96b9-32d5dbbcf9cb | 2026-07-29 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| DECONIMO Reconstitution | DECONIMO RECONSTITUTION | Image Amazon LLC | 57ab9b1c-9a18-3786-e063-6394a90a2c63 | 2026-07-28 | Warnings | 059QF0KO0R |
| aripiprazole | ARIPIPRAZOLE | REMEDYREPACK INC. | 1ad7d167-1235-4c5c-8159-da8972240ede | 2026-07-27 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Droptics Dry Eye Relief | CARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80 | Droptics LLC | 29d7614b-f4b7-48e2-97c5-d1bff27731d2 | 2026-07-22 | Warnings | K679OBS311 |
| Aripiprazole | ARIPIPRAZOLE | REMEDYREPACK INC. | 119e3387-39a2-4fe5-904b-c2d008425c0a | 2026-07-22 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Sterile Water | WATER | Cardinal Health 107, LLC | 9655cd02-82b5-4a75-813b-854b19551481 | 2026-07-21 | Warnings, Adverse reactions | 059QF0KO0R |
| Aripiprazole | ARIPIPRAZOLE ORALLY DISINTEGRATING | Dr. Reddy's Laboratories Inc | 394ea4a4-3991-4f98-b38f-56e9335d66b3 | 2026-07-21 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | REMEDYREPACK INC. | 99747897-22fe-4bee-9942-6349c0c8f6b0 | 2026-07-17 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE ORAL | ATLANTIC BIOLOGICALS CORP. | 042b725c-1c17-4cfb-80b2-c841226d795e | 2026-07-10 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Coupler LLC | 56439ef6-a07e-34c9-e063-6294a90a77c3 | 2026-07-10 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Coupler LLC | 55f3a705-9412-0f88-e063-6294a90a2b53 | 2026-07-06 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Aripiprazole | ARIPIPRAZOLE | Coupler LLC | 55f446b0-caa2-aca8-e063-6294a90af441 | 2026-07-06 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Retaine CMC | CARBOXYMETHYLCELLULOSE SODIUM | OCuSOFT LLC | a3698c71-0c80-4246-be52-5e7d96f6c540 | 2026-07-06 | Warnings | K679OBS311 |
| Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g) | NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE) | Reedfresh Co., LTD | 55d703ca-ff9d-0dbc-e063-6294a90ab6b1 | 2026-07-05 | Warnings | 059QF0KO0R |
| Aripiprazole | ARIPIPRAZOLE | REMEDYREPACK INC. | a1191a90-eb83-4a59-948c-b9774d2c83a5 | 2026-07-02 | Boxed warning, Warnings, Adverse reactions | 82VFR53I78 |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Protective Industrial Products, Inc. | 558e5926-9027-d3f6-e063-6294a90ab121 | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |