NDC 68788-8757-03 - Ibuprofen
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
- 68788-8757
- Requested NDC
- 68788-8757-03
- Package NDCs from labels
- 68788-8757-4, 68788-8757-2, 68788-8757-7, 68788-8757-3, 68788-8757-5, 68788-8757-6, 68788-8757-9, 68788-8757-1, 68788-8757-8, 68788-8757-03
- Manufacturer
- Preferred Pharmaceuticals Inc.
- Effective date
- 2026-01-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen Tablets, USP 400 mg, 600 mg and 800 mg | Preferred Pharmaceuticals Inc. | 2026-01-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68788-8757-1 | Ibuprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 2 | |
| 68788-8757-2 | Ibuprofen | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | 2 | |
| 68788-8757-3 | Ibuprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 2 | |
| 68788-8757-4 | Ibuprofen | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | 2 | |
| 68788-8757-5 | Ibuprofen | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | 2 | |
| 68788-8757-6 | Ibuprofen | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 2 | |
| 68788-8757-7 | Ibuprofen | 21 in 1 BOTTLE | TABLET, FILM COATED | 21 | 2 | |
| 68788-8757-8 | Ibuprofen | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | 2 | |
| 68788-8757-9 | Ibuprofen | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68788-8757 | IBUPROFEN TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.] | 1 | Current NDC, 9 package rows | 20241019_b84ea215-e61d-4c00-8a34-d47c4080779b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68788-8757-1 | EA - Each | 68788-8757 | 7af27744-ba21-4787-abc8-a77b525a5df8 | 1 | 2025-01-14 |
| 68788-8757-2 | EA - Each | 68788-8757 | 10ba1ef3-0e87-481d-bad8-ab85f68ea87a | 1 | 2025-01-14 |
| 68788-8757-3 | EA - Each | 68788-8757 | 9c819978-1cd2-476c-abd0-e06a1a6e5ac4 | 1 | 2025-01-14 |
| 68788-8757-4 | EA - Each | 68788-8757 | 6dd19a21-015d-4f46-912c-3fabfe5b0c7e | 1 | 2025-01-14 |
| 68788-8757-5 | EA - Each | 68788-8757 | bc9cc155-4c88-41ee-8d9b-60d1dfedb835 | 1 | 2025-01-14 |
| 68788-8757-6 | EA - Each | 68788-8757 | 61f119c3-007f-4057-a34e-3a793bb5908c | 1 | 2025-01-14 |
| 68788-8757-7 | EA - Each | 68788-8757 | fac81f84-f707-4763-9619-36fee2778b3a | 1 | 2025-01-14 |
| 68788-8757-8 | EA - Each | 68788-8757 | 2313c509-2442-4ae9-af4a-0c7c2e86aa89 | 1 | 2025-01-14 |
| 68788-8757-9 | EA - Each | 68788-8757 | 5fc08f1e-a489-4485-97f0-8b1bee1cff61 | 1 | 2025-01-14 |
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 |
|---|---|---|---|---|---|---|
| Lymph Tonic II | ECHINACEA (ANGUSTIFOLIA), COLLINSONIA CANADENSIS, PHYTOLACCA DECANDRA, KALI IODATUM, PINUS SYLVESTRIS, PIX LIQUIDA, FERRUM PHOSPHORICUM, AESCULUS HIPPOCASTANUM, BARYTA CARBONICA, BERBERIS VULGARIS, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CAUSTICUM, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, STELLARIA MEDIA, SULPHUR, TEREBINTHINA, THUJA OCCIDENTALIS, BUFO RANA | BioActive Nutritional, Inc. | 0e3265b0-b210-4a4c-80d2-8a9712981d4e | 2026-09-17 | Warnings | ETJ7Z6XBU4 |
| dual action | ACETAMINOPHEN, IBUPROFEN | Rite Aid Corporation | 54b08d24-d5e9-4111-9d97-329896e8309d | 2026-09-09 | Warnings | WK2XYI10QM |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | W Aesthetics | 5b0f2c8f-d6fa-5e25-e063-6394a90a084d | 2026-09-09 | Warnings | 15FIX9V2JP |
| Ibuprofen | IBUPROFEN | Lidl US LLC | 0ca02f8b-4413-4e7c-a67b-8c67c53e1343 | 2026-09-09 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | GOODSENSE | 596a1007-08ea-00ec-e063-6394a90a5eb2 | 2026-09-09 | Warnings | WK2XYI10QM |
| ibuprofen childrens | IBUPROFEN | Rite Aid Corporation | c6e68886-edcb-414d-9cba-0d97772ef8b6 | 2026-09-09 | Warnings | WK2XYI10QM |
| Ibuprofen minis | IBUPROFEN | The Kroger Co. | 15709fa7-114b-453c-b63d-f1c4f28f0f95 | 2026-09-08 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 2144eff0-d7ab-486d-b116-a4ff3ae2afe2 | 2026-09-08 | Boxed warning, Warnings, Adverse reactions | 197806 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | The Kroger Co. | a7789f7f-3356-463b-9fd7-2d7f7eba2799 | 2026-09-08 | Warnings | WK2XYI10QM |
| IBUPROFEN | IBUPROFEN | Amazon.com Services LLC | 90659e83-d989-46a5-9680-3a4f61612511 | 2026-09-04 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Direct_Rx | 40071818-5bf0-095b-e063-6294a90ad58a | 2026-09-04 | Boxed warning, Warnings, Adverse reactions | 197806 WK2XYI10QM |
| Psoriasis Control | CENTELLA ASIATICA, SODIUM CHLORIDE, AND SILICON DIOXIDE | Forces of Nature | 2db33771-0bb9-49f8-84fa-dddc28e4ba26 | 2026-09-04 | Warnings | ETJ7Z6XBU4 |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 8d518a08-486a-4d11-b042-27fc1e6060c9 | 2026-09-03 | Warnings | WK2XYI10QM |
| IBUPROFEN Immediate Release | IBUPROFEN | Strides Pharma Inc | a5dd275f-f388-44ec-8297-74430a742d52 | 2026-09-02 | Boxed warning, Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 0fa4cd66-66ad-4ec9-b38c-6b5840df39df | 2026-09-02 | Boxed warning, Warnings, Adverse reactions | ANDA202413 197805 WK2XYI10QM |
| Ibuprofen Immediate Release | IBUPROFEN | Strides Pharma Inc | ebcc4da3-d0f6-4e40-99b5-e88310ea4a5b | 2026-09-02 | Boxed warning, Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 99730c4a-d2ee-46f5-91f4-a15cbaace40d | 2026-09-01 | Boxed warning, Warnings, Adverse reactions | 197806 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 3a38add6-a114-4e18-836c-3bfc727db231 | 2026-09-01 | Boxed warning, Warnings, Adverse reactions | ANDA202413 197807 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 404df13d-4ada-4324-9eed-e21f5d5043a4 | 2026-09-01 | Boxed warning, Warnings, Adverse reactions | ANDA202413 197807 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | fef89d3f-16e1-4a76-aabd-11d6eca4be86 | 2026-09-01 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.