NDC 51672-1385-08 - 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
- 51672-1385
- Requested NDC
- 51672-1385-08
- Package NDCs from labels
- 51672-1385-8, 51672-1385-9, 51672-1385-08
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-03-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen Oral Suspension USP, 100 mg/5 mL | REMEDYREPACK INC. | 2026-03-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Ibuprofen Oral Suspension USP, 100 mg/5 mL | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-12-27 | HUMAN PRESCRIPTION DRUG LABEL |
| Ibuprofen Oral Suspension USP, 100 mg/5 mL | Pharmaceutical Associates, Inc. | 2024-11-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Ibuprofen Oral Suspension USP, 100 mg/5 mL | Preferred Pharmaceuticals Inc. | 2020-06-11 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-1385-8 | Ibuprofen | 1 in 1 CARTON | SUSPENSION | 1 | 8 | |
| 51672-1385-8 | Ibuprofen | 118 mL in 1 BOTTLE | SUSPENSION | 118 | 8 | |
| 51672-1385-9 | Ibuprofen | 473 mL in 1 BOTTLE | SUSPENSION | 473 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-1385 | IBUPROFEN SUSPENSION [SUN PHARMACEUTICAL INDUSTRIES, INC.] | 6 | Current NDC, Legacy NDC, 3 package rows | 20250406_a8b46ae5-67bc-494d-850e-b4e4ed5a33b3.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-1385-8 | ML - Milliliter | 51672-1385 | 13a2a3e8-f834-4d2d-a6b8-b343115b264c | 1 | 2017-10-13 |
| 51672-1385-9 | ML - Milliliter | 51672-1385 | 7c8f4189-f5ee-4e29-8c05-9539e9dfe33f | 1 | 2017-10-13 |
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 |
|---|---|---|---|---|---|---|
| Ibuprofen | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 3c1c1b65-f57f-62b0-e063-6294a90a1021 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 3802982a-2373-9ca3-e063-6394a90a0ab7 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 4573753d-117b-a6f2-e063-6394a90ae2f9 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 3ed7faff-fd48-0a83-e063-6394a90aab14 | 2026-06-23 | Warnings | WK2XYI10QM |
| Pain Relief | IBUPROFEN | Albertsons Companies | f9deaeb7-efb3-4019-e053-6394a90a33d6 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | MEIJER DISTRIBUTION INC. | bc15fea8-0d86-4546-e053-2995a90abee3 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | MEIJER DISTRIBUTION INC. | a13ac87b-b395-685e-e053-2a95a90ab5d3 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Whole Foods Market, INC. | 32348505-744c-fbfd-e063-6394a90a82d7 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | AMERISOURCE BERGEN | 1afcf0c6-bd41-4621-9e44-d97b81221c12 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | AMERISOURCE BERGEN | a13cee82-1c4e-0cbe-e053-2a95a90a3ab8 | 2026-06-23 | Warnings | WK2XYI10QM |
| Bacteriostatic Water | BACTERIOSTATIC WATER | Fujian Genohope Biotech Ltd. | 54f66b82-c9e5-a2bc-e063-6394a90adbbc | 2026-06-23 | 059QF0KO0R | |
| Ibuprofen | IBUPROFEN | A-S Medication Solutions | 51de1183-d226-4869-a00a-f6c74e126a39 | 2026-06-23 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | A-S Medication Solutions | 25a94943-9acc-49c8-a4da-7e07bb2c35eb | 2026-06-23 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Topco Associates, LLC | 59a88ca7-eb37-46de-9134-a5a6d330bd49 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen Famotidine | IBUPROFEN FAMOTIDINE | Direct_Rx | 54d9e1fc-507d-1859-e063-6394a90a8c6b | 2026-06-22 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Cardinal Health 107, LLC | 8ea0e303-3967-4d71-8255-ac42a841ce28 | 2026-06-22 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Rohto Cool Relief | NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80 | The Mentholatum Company | dc8f1ff3-87ae-47ca-815f-5a0e34f8cf30 | 2026-06-19 | Warnings | 6OZP39ZG8H |
| Ibuprofen and Famotidine | IBUPROFEN AND FAMOTIDINE | Advanced Rx of Tennessee, LLC | 548c705e-4094-fc6f-e063-6394a90a3426 | 2026-06-18 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | L.N.K. International, Inc. | 027ded51-aa01-6619-3938-c8162a421cf3 | 2026-06-18 | Warnings | WK2XYI10QM |
| Humalog | INSULIN LISPRO | Eli Lilly and Company | c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f | 2026-06-16 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.