NDC 51672-2144-01 - 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
- 51672-2144
- Requested NDC
- 51672-2144-01
- Package NDCs from labels
- 51672-2144-8, 51672-2144-1, 51672-2144-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2025-07-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-07-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2144-1 | Ibuprofen | 240 mL in 1 BOTTLE | SUSPENSION | 240 | 5 | |
| 51672-2144-1 | Ibuprofen | 1 in 1 CARTON | SUSPENSION | 1 | 5 | |
| 51672-2144-8 | Ibuprofen | 120 mL in 1 BOTTLE | SUSPENSION | 120 | 5 | |
| 51672-2144-8 | Ibuprofen | 1 in 1 CARTON | SUSPENSION | 1 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2144 | IBUPROFEN SUSPENSION [-SUN PHARMACEUTICAL INDUSTRIES, INC.] | 4 | Current NDC, Legacy NDC, 4 package rows | 20250406_6cf3328b-da8f-4f6b-8237-16a4d6b9c833.zip |
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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Medical Purchasing Solutions, LLC | e90b47e3-9636-b9ee-e053-2a95a90ad48c | 2022-09-19 | Warnings, Adverse reactions | 059QF0KO0R |
| REFRESH OPTIVE Advanced | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 | Allergan, Inc. | ebd0839e-2e1d-4e0e-986c-19f1f5c76358 | 2022-09-15 | Warnings | PDC6A3C0OX 6OZP39ZG8H |
| Ibuprofen | IBUPROFEN | Aurohealth LLC | e1b49257-d226-457f-8f2d-9a757a65bbcb | 2022-09-06 | Warnings | WK2XYI10QM |
| REFRESH OPTIVE Advanced | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80 | Allergan, Inc. | aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0 | 2022-09-01 | Warnings | PDC6A3C0OX 6OZP39ZG8H |
| Childrens Ibuprofen Oral Suspension | IBUPROFEN | Pharmaceutical Associates, Inc. | 7a6832f2-2d80-483c-bde3-e6cacb7c318a | 2022-08-31 | Warnings | 197803 WK2XYI10QM |
| betr pain relief | IBUPROFEN | Live Betr LLC | 1b709dce-5c71-45e6-b516-d510a0a8c25d | 2022-08-24 | Warnings | WK2XYI10QM |
| Diphenhydramine HCl and Ibuprofen | DIPHENHYDRAMINE HCL AND IBUPROFEN | Aurohealth LLC | 2c7c5349-06c9-401a-88e9-8f91ddb7f91a | 2022-08-19 | Warnings | WK2XYI10QM |
| Ibuprofen Oral | IBUPROFEN ORAL | Strategic Sourcing Services | a3062142-db0e-4758-a762-2b2bb05670b1 | 2022-08-10 | Warnings | 197803 WK2XYI10QM |
| Ibuprofen | IBUPROFEN TABLET, FILM-COATED | Lil' Drug Store Products, Inc. | e5bf5e09-7d42-6314-e053-2a95a90a2325 | 2022-08-08 | Warnings | WK2XYI10QM |
| Glycerinum | GLYCERINUM | Hahnemann Laboratories, INC. | e34f8796-85b5-2946-e053-2995a90a251e | 2022-07-08 | PDC6A3C0OX | |
| Ibuprofen | IBUPROFEN | DOLGENCORP, INC. | df321783-73cb-55bf-e053-2a95a90a4ce2 | 2022-07-07 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Proficient Rx LP | b7565aac-a928-4116-b9af-cf636da4537c | 2022-07-01 | Warnings | ANDA209207 197803 WK2XYI10QM |
| REFRESH Optive Mega-3 | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 | Allergan, Inc. | c5f2b3f2-2071-45bd-a010-67f848bc0233 | 2022-06-30 | Warnings | PDC6A3C0OX 6OZP39ZG8H |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | f42ac50f-0ec5-4713-a4c8-99d972d90bed | 2022-06-22 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | e71c6c83-d518-496c-b2ab-efd5987e4783 | 2022-06-09 | Warnings, Adverse reactions | 059QF0KO0R |
| Ibuprofen and Diphenhydramine Citrate | IBUPROFEN AND DIPHENHYDRAMINE CITRATE | Aurohealth LLC | 21c1f5c5-19fa-4a59-bad3-ea85fd37471b | 2022-06-03 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | CARDINAL HEALTH | dfbbde4f-633d-6d57-e053-2a95a90ad82f | 2022-05-24 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Aurohealth LLC | 7779c369-50bf-4cde-9015-ff3fb35e128e | 2022-05-16 | Warnings | WK2XYI10QM |
| Addiclenz | BETA VULGARIS, BOLDO, CHELIDONIUM MAJUS, PETROSELINUM SATIVUM, TARAXACUM OFFICINALE, ARSENICUM ALBUM, BISPHENOL A, COBALTUM METALLICUM, CUPRUM METALLICUM, GLYPHOSATE, IODIUM, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, SELENIUM METALLICUM, ZINCUM METALLICUM, ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYL PARABEN, PROPYL PARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM | Deseret Biologicals, Inc. | e39235ea-2a2f-44a7-92d6-fb1d428ebabd | 2022-05-12 | Warnings | OJ245FE5EU |
| Ibuprofen | IBUPROFEN | Proficient Rx LP | d2c7f045-e70c-4e2b-b2e0-d81a271d0a04 | 2022-05-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.